A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099481



Internal ID15605981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150856387..150863234hg38UCSC Ensembl
Innerchr7:150553475..150560322hg19UCSC Ensembl
Innerchr7:150184408..150191255hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386848
hg196848
hg186848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608993
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)nssv1099481
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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