A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018868



Internal ID18761401
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 StatusM
Merged Variantsdgv6523n100
Supporting Variantsnssv3655190
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)nsv1018868
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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