A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv906873



Internal ID15854143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38572678..38635081hg38UCSC Ensembl
Innerchr2:38799820..38862223hg19UCSC Ensembl
Innerchr2:38653324..38715727hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3862404
hg1962404
hg1862404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581483
Supporting Variants
Samples
Known GenesHNRNPLL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv906873
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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