A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176119



Internal ID15880522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111664695..111715190hg38UCSC Ensembl
Innerchr9:114426975..114477470hg19UCSC Ensembl
Innerchr9:113466796..113517291hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3850496
hg1950496
hg1850496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615193
Supporting Variants
SamplesNINDS_222
Known GenesC9orf84, DNAJC25-GNG10, GNG10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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