A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1081514



Internal ID15588014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27162670..27241685hg38UCSC Ensembl
Innerchr7:27202289..27281304hg19UCSC Ensembl
Innerchr7:27168814..27247829hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3879016
hg1979016
hg1879016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606468
Supporting Variants
Samples
Known GenesHOTTIP, HOXA10, HOXA10-HOXA9, HOXA11, HOXA11-AS, HOXA13, HOXA9, HOXA-AS4, MIR196B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1081514
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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