A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv904248



Internal ID16198204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18834890..19050777hg38UCSC Ensembl
Innerchr2:19016156..19250533hg19UCSC Ensembl
Innerchr2:18879637..19114014hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38215888
hg19234378
hg18234378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581117
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)nssv904248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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