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15q15.3 deletion AND Autosomal dominant nonsyndromic hearing loss 16

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Feb 19, 2016
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000225051.1

Allele description [Variation Report for 15q15.3 deletion]

15q15.3 deletion

Gene:
STRC:stereocilin [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
15q15.3
Preferred name:
15q15.3 deletion

Condition(s)

Name:
Autosomal dominant nonsyndromic hearing loss 16
Synonyms:
Deafness, autosomal dominant 16
Identifiers:
MONDO: MONDO:0011389; MedGen: C1858916; Orphanet: 90635; OMIM: 603964

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000282019Laboratory of Prof. Karen Avraham, Tel Aviv University
no assertion criteria provided
Pathogenic
(Feb 19, 2016)
germlineresearch

Description

NSHL; recessive, DFNB160.1 MB deletion

SCV000282019

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedresearch

Details of each submission

From Laboratory of Prof. Karen Avraham, Tel Aviv University, SCV000282019.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedresearchnot provided

Description

Congenital, moderate HL

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 23, 2022