A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613139



Internal ID16400548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2689244..2710537hg38UCSC Ensembl
Innerchr9:2689244..2710537hg19UCSC Ensembl
Innerchr9:2679244..2700537hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3821294
hg1921294
hg1821294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12478n54
Supporting Variantsnssv1126222
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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