A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126087



Internal ID15979273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2012767..2059341hg38UCSC Ensembl
Innerchr9:2012767..2059341hg19UCSC Ensembl
Innerchr9:2002767..2049341hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3846575
hg1946575
hg1846575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613079
Supporting Variants
Samples
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126087
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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