A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605974



Internal ID16393383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4455370..4606619hg38UCSC Ensembl
Innerchr7:4495001..4646250hg19UCSC Ensembl
Innerchr7:4461527..4612776hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38151250
hg19151250
hg18151250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155140
SamplesHGDP01162
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605974
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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