A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615885



Internal ID16403294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135548993..135549504hg38UCSC Ensembl
Innerchr9:138440839..138441350hg19UCSC Ensembl
Innerchr9:137580660..137581171hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38512
hg19512
hg18512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1147140, nssv1147141, nssv1147139, nssv1147138
Samples
Known GenesOBP2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615885
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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