A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176508



Internal ID15525985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130226430..130263670hg38UCSC Ensembl
Innerchr9:132988709..133025949hg19UCSC Ensembl
Innerchr9:132028530..132065770hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3837241
hg1937241
hg1837241
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615504
Supporting Variants
SamplesHGDP00011
Known GenesNCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176508
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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