A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655218



Internal ID18953499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89699437..89927701hg38UCSC Ensembl
Innerchr7:89328751..89557015hg19UCSC Ensembl
Innerchr7:89166687..89394951hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38228265
hg19228265
hg18228265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033642
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)nssv3655218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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