A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099498



Internal ID15605998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150901404..150970122hg38UCSC Ensembl
Innerchr7:150598492..150667210hg19UCSC Ensembl
Innerchr7:150229425..150298143hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3868719
hg1968719
hg1868719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609000
Supporting Variants
Samples
Known GenesKCNH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099498
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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