A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614520



Internal ID16401929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62090746..62138345hg38UCSC Ensembl
Innerchr9:67517803..67565410hg19UCSC Ensembl
Innerchr9:67107623..67155230hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3847600
hg1947608
hg1847608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134720
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614520
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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