A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141235



Internal ID15647735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111483503..111484177hg38UCSC Ensembl
Innerchr9:114245783..114246457hg19UCSC Ensembl
Innerchr9:113285604..113286278hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38675
hg19675
hg18675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615190
Supporting Variants
Samples
Known GenesKIAA0368
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141235
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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