A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655190



Internal ID18606785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88010584..88042439hg38UCSC Ensembl
Innerchr7:87639899..87671754hg19UCSC Ensembl
Innerchr7:87477835..87509690hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3831856
hg1931856
hg1831856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018868
Supporting Variants
Samples
Known GenesADAM22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655190
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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