A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613090



Internal ID16400499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2137725..2157934hg38UCSC Ensembl
Innerchr9:2137725..2157934hg19UCSC Ensembl
Innerchr9:2127725..2147934hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3820210
hg1920210
hg1820210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156432
SamplesNINDS_104
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613090
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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