A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903225



Internal ID16197181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4165788..4641119hg38UCSC Ensembl
Innerchr2:4213378..4688709hg19UCSC Ensembl
Innerchr2:4191253..4666584hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38475332
hg19475332
hg18475332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580845
Supporting Variants
Samples
Known GenesLOC727982
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv903225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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