A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615190



Internal ID16055913
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141237, nssv1141234, nssv1141236, nssv1141235, nssv1141238, nssv1141233
Samples
Known GenesKIAA0368
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615190
Frequency
Sample Size17421
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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