A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701140



Internal ID15437792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100980983..100984280hg38UCSC Ensembl
Innerchr3:100699827..100703124hg19UCSC Ensembl
Innerchr3:102182517..102185814hg18UCSC Ensembl
Innerchr3:102182517..102185814hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg383298
hg193298
hg183298
hg173298
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525082
Supporting Variants
Samples
Known GenesABI3BP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701140
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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