A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614562



Internal ID16401971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69280692..69283611hg38UCSC Ensembl
Innerchr9:71895608..71898527hg19UCSC Ensembl
Innerchr9:71085428..71088347hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382920
hg192920
hg182920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12742n54
Supporting Variantsnssv1137085, nssv1137084
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614562
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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