A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903701



Internal ID16197657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10011618..10015790hg38UCSC Ensembl
Innerchr2:10151745..10155917hg19UCSC Ensembl
Innerchr2:10069196..10073368hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg384173
hg194173
hg184173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580962
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)nssv903701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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