A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615498



Internal ID16402907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130107065..130182266hg38UCSC Ensembl
Innerchr9:132869344..132944545hg19UCSC Ensembl
Innerchr9:131909165..131984366hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3875202
hg1975202
hg1875202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176504
SamplesHGDP00189
Known GenesGPR107, NCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615498
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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