A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605867



Internal ID16046590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2629953..2705490hg38UCSC Ensembl
Innerchr7:2669587..2745124hg19UCSC Ensembl
Innerchr7:2636113..2711650hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3875538
hg1975538
hg1875538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11144n54
Supporting Variantsnssv1155114
SamplesHGDP00852
Known GenesAMZ1, TTYH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605867
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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