A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608349



Internal ID16395758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:125700587..126208797hg38UCSC Ensembl
Innerchr7:125340641..125848851hg19UCSC Ensembl
Innerchr7:125127877..125636087hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38508211
hg19508211
hg18508211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093608
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608349
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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