A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606463



Internal ID16047186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27095695..27142626hg38UCSC Ensembl
Innerchr7:27135314..27182245hg19UCSC Ensembl
Innerchr7:27101839..27148770hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3846932
hg1946932
hg1846932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11244n54
Supporting Variantsnssv1081509
Samples
Known GenesHOTAIRM1, HOXA1, HOXA2, HOXA3, HOXA4, HOXA5, HOXA-AS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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