A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176007



Internal ID15533900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135491367..135577889hg38UCSC Ensembl
Innerchr9:138383213..138469735hg19UCSC Ensembl
Innerchr9:137523034..137609556hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3886523
hg1986523
hg1886523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615882
Supporting Variants
SamplesNINDS_230
Known GenesC9orf116, LCN1, LOC100130954, MRPS2, OBP2A, PAEP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176007
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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