A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903719



Internal ID15850989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11724820..11758805hg38UCSC Ensembl
Innerchr2:11864946..11898931hg19UCSC Ensembl
Innerchr2:11782397..11816382hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3833986
hg1933986
hg1833986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580973
Supporting Variants
Samples
Known GenesLPIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv903719
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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