A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677597



Internal ID15414249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162412903..162459502hg38UCSC Ensembl
Innerchr3:162130691..162177290hg19UCSC Ensembl
Innerchr3:163613385..163659984hg18UCSC Ensembl
Innerchr3:163613393..163659992hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3846600
hg1946600
hg1846600
hg1746600
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)nssv677597
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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