A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613107



Internal ID16400516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2148877..2151371hg38UCSC Ensembl
Innerchr9:2148877..2151371hg19UCSC Ensembl
Innerchr9:2138877..2141371hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382495
hg192495
hg182495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12475n54
Supporting Variantsnssv1126185, nssv1126181, nssv1126184, nssv1126182, nssv1126179, nssv1126180, nssv1126178, nssv1126176, nssv1126175, nssv1126183, nssv1126177
Samples
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613107
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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