A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614649



Internal ID16402058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73404155..73412434hg38UCSC Ensembl
Innerchr9:76019071..76027350hg19UCSC Ensembl
Innerchr9:75208891..75217170hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388280
hg198280
hg188280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12756n54
Supporting Variantsnssv1137309
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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