A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661533



Internal ID18959814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..62316440hg38UCSC Ensembl
Innerchr7:61063962..61760691hg19UCSC Ensembl
Innerchr7:61067904..61398126hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381235204
hg19696730
hg18330223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018596
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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