A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078809



Internal ID15931995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5072923..5137521hg38UCSC Ensembl
Innerchr7:5112554..5177152hg19UCSC Ensembl
Innerchr7:5079080..5143678hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3864599
hg1964599
hg1864599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605981
Supporting Variants
Samples
Known GenesRBAKDN, RBAK-RBAKDN, ZNF890P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078809
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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