A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705296



Internal ID15441948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75408707..75519068hg38UCSC Ensembl
Innerchr3:75457858..75568219hg19UCSC Ensembl
Innerchr3:75540548..75650909hg18UCSC Ensembl
Innerchr3:75540548..75650909hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38110362
hg19110362
hg18110362
hg17110362
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517173
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705296
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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