A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643406



Internal ID18941687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35508158..35586719hg38UCSC Ensembl
Innerchr7:35547768..35626329hg19UCSC Ensembl
Innerchr7:35514293..35592854hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3878562
hg1978562
hg1878562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030385
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)nssv3643406
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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