A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614447



Internal ID16401856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42826529..42827459hg38UCSC Ensembl
Innerchr9:44143660..44144590hg19UCSC Ensembl
Innerchr9:44083656..44084586hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38931
hg19931
hg18931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134494, nssv1134495
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614447
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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