A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606466



Internal ID16047189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27105405..27157700hg38UCSC Ensembl
Innerchr7:27145024..27197319hg19UCSC Ensembl
Innerchr7:27111549..27163844hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3852296
hg1952296
hg1852296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11244n54
Supporting Variantsnssv1081512
Samples
Known GenesHOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA-AS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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