A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613259



Internal ID16400668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7032776..7541338hg38UCSC Ensembl
Innerchr9:7032776..7541338hg19UCSC Ensembl
Innerchr9:7022776..7531338hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38508563
hg19508563
hg18508563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126849
Samples
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613259
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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