A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1084627



Internal ID15937813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53194358..53502452hg38UCSC Ensembl
Innerchr7:53262051..53570145hg19UCSC Ensembl
Innerchr7:53229545..53537639hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38308095
hg19308095
hg18308095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607010
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)nssv1084627
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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