A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1097886



Internal ID15951072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:145220724..145226205hg38UCSC Ensembl
Innerchr7:144917817..144923298hg19UCSC Ensembl
Innerchr7:144548750..144554231hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385482
hg195482
hg185482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608915
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1097886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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