A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615188



Internal ID16055911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111476546..111484060hg38UCSC Ensembl
Innerchr9:114238826..114246340hg19UCSC Ensembl
Innerchr9:113278647..113286161hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg387515
hg197515
hg187515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141230
Samples
Known GenesKIAA0368
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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