A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606464



Internal ID16047187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27098859..27128971hg38UCSC Ensembl
Innerchr7:27138478..27168590hg19UCSC Ensembl
Innerchr7:27105003..27135115hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3830113
hg1930113
hg1830113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1081510
Samples
Known GenesHOTAIRM1, HOXA2, HOXA3, HOXA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606464
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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