A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606465



Internal ID16047188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27104138..27189930hg38UCSC Ensembl
Innerchr7:27143757..27229549hg19UCSC Ensembl
Innerchr7:27110282..27196074hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3885793
hg1985793
hg1885793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081511
Samples
Known GenesHOXA10, HOXA10-HOXA9, HOXA11, HOXA11-AS, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, HOXA-AS3, HOXA-AS4, MIR196B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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