A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606285



Internal ID16393694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14968513..15058379hg38UCSC Ensembl
Innerchr7:15008138..15098004hg19UCSC Ensembl
Innerchr7:14974663..15064529hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3889867
hg1989867
hg1889867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079288
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606285
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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