A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661677



Internal ID18959958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..62933040hg38UCSC Ensembl
Innerchr7:61840313..62393418hg19UCSC Ensembl
Innerchr7:61477748..62030853hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38426261
hg19553106
hg18553106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017338
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)nssv3661677
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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