A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679612



Internal ID15069578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73790158..73888491hg38UCSC Ensembl
Innerchr10:75549916..75648249hg19UCSC Ensembl
Innerchr10:75219922..75318255hg18UCSC Ensembl
Innerchr10:75219922..75318255hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3898334
hg1998334
hg1898334
hg1798334
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517549
Supporting Variants
Samples
Known GenesCAMK2G, NDST2, ZSWIM8, ZSWIM8-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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