A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608227



Internal ID16395636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113268733..113349717hg38UCSC Ensembl
Innerchr7:112908788..112989772hg19UCSC Ensembl
Innerchr7:112696024..112777008hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3880985
hg1980985
hg1880985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155385
Samples1780862576_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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