A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606156



Internal ID16393565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9337425..9376645hg38UCSC Ensembl
Innerchr7:9377055..9416275hg19UCSC Ensembl
Innerchr7:9343580..9382800hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3839221
hg1939221
hg1839221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155266
SamplesNINDS_234
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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