A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613173



Internal ID16053896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4730743..4758022hg38UCSC Ensembl
Innerchr9:4730743..4758022hg19UCSC Ensembl
Innerchr9:4720743..4748022hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3827280
hg1927280
hg1827280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156208
Samples1780854296_A
Known GenesAK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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