A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605975



Internal ID16393384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4568543..4629505hg38UCSC Ensembl
Innerchr7:4608174..4669136hg19UCSC Ensembl
Innerchr7:4574700..4635662hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3860963
hg1960963
hg1860963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155141
SamplesHGDP00127
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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