A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655189



Internal ID18953470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87289287..87337403hg38UCSC Ensembl
Innerchr7:86918603..86966719hg19UCSC Ensembl
Innerchr7:86756539..86804655hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3848117
hg1948117
hg1848117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022111
Supporting Variants
Samples
Known GenesTP53TG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655189
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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