A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126183



Internal ID15979369
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 StatusS
Merged Variantsnsv613107
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)nssv1126183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer