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nsv5485948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 337 SVs from 61 studies. See in: genome view    
Submitted genomic73,203,779-73,296,779Question Mark
Overlapping variant regions from other studies: 93 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):733,015-826,015Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr773,203,77973,296,779
nsv5485948RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871064.1Chr7|NW_00
3871064.1
733,015826,015

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16998077duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16998077Submitted genomicNC_000007.14:g.732
03779_73296779dup
GRCh38 (hg38)NC_000007.14Chr773,203,77973,296,779
nssv16998077RemappedPerfectNW_003871064.1:g.7
33015_826015dup
GRCh37.p13First PassNW_003871064.1Chr7|NW_00
3871064.1
733,015826,015

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv169980770.002126190
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