A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656229



Internal ID18954510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109339142..109463293hg38UCSC Ensembl
Innerchr7:108979199..109103350hg19UCSC Ensembl
Innerchr7:108766435..108890586hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38124152
hg19124152
hg18124152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026963
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)nssv3656229
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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