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nsv6147148

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,904

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 79 SVs from 25 studies. See in: genome view    
Submitted genomic29,992,070-29,999,973Question Mark
Overlapping variant regions from other studies: 79 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):30,033,561-30,041,464Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147148Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr329,992,07029,999,973
nsv6147148RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr330,033,56130,041,464

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16931366mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16931366Submitted genomicNC_000003.12:g.299
92070_29999973del
GRCh38 (hg38)NC_000003.12Chr329,992,07029,999,973
nssv16931366RemappedPerfectNC_000003.11:g.300
33561_30041464del
GRCh37.p13First PassNC_000003.11Chr330,033,56130,041,464

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)
nssv16931366<0.00116404
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