A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642986



Internal ID18941267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12703967..12887484hg38UCSC Ensembl
Innerchr7:12743592..12927109hg19UCSC Ensembl
Innerchr7:12710117..12893634hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38183518
hg19183518
hg18183518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027501
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)nssv3642986
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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