A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654232



Internal ID18952513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3085878..3164888hg38UCSC Ensembl
Innerchr7:3125512..3204521hg19UCSC Ensembl
Innerchr7:3092038..3171047hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3879011
hg1979010
hg1879010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020680
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)nssv3654232
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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