A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698561



Internal ID15435213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36344330..36363072hg38UCSC Ensembl
Innerchr3:36385822..36404564hg19UCSC Ensembl
Innerchr3:36360826..36379568hg18UCSC Ensembl
Innerchr3:36360826..36379568hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3818743
hg1918743
hg1818743
hg1718743
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522903
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698561
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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