A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv907890



Internal ID15855160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43226244..43227591hg38UCSC Ensembl
Innerchr2:43453383..43454730hg19UCSC Ensembl
Innerchr2:43306887..43308234hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381348
hg191348
hg181348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581653
Supporting Variants
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv907890
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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