A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099491



Internal ID15605991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150856517..150875294hg38UCSC Ensembl
Innerchr7:150553605..150572382hg19UCSC Ensembl
Innerchr7:150184538..150203315hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3818778
hg1918778
hg1818778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608996
Supporting Variants
Samples
Known GenesAOC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099491
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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