A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661231



Internal ID18959512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:46832196..46849893hg38UCSC Ensembl
Innerchr7:46871794..46889491hg19UCSC Ensembl
Innerchr7:46838319..46856016hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3817698
hg1917698
hg1817698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020204
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)nssv3661231
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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