A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904430



Internal ID16198386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22292479..22382758hg38UCSC Ensembl
Innerchr2:22515351..22605630hg19UCSC Ensembl
Innerchr2:22368856..22459135hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3890280
hg1990280
hg1890280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581172
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv904430
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