A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655692



Internal ID18607287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:71247382..71292943hg38UCSC Ensembl
Innerchr7:70712368..70757929hg19UCSC Ensembl
Innerchr7:70350304..70395865hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3845562
hg1945562
hg1845562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033155
Supporting Variants
Samples
Known GenesWBSCR17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655692
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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