A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704826



Internal ID15441478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162413620..162415287hg38UCSC Ensembl
Innerchr3:162131408..162133075hg19UCSC Ensembl
Innerchr3:163614102..163615769hg18UCSC Ensembl
Innerchr3:163614110..163615777hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381668
hg191668
hg181668
hg171668
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704826
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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