A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608229



Internal ID16395638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113647336..113699120hg38UCSC Ensembl
Innerchr7:113287391..113339175hg19UCSC Ensembl
Innerchr7:113074627..113126411hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3851785
hg1951785
hg1851785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092749
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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