A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613112



Internal ID16400521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2148966..2150862hg38UCSC Ensembl
Innerchr9:2148966..2150862hg19UCSC Ensembl
Innerchr9:2138966..2140862hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381897
hg191897
hg181897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12474n54
Supporting Variantsnssv1126194, nssv1126195, nssv1126193
Samples
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613112
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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