A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009434



Internal ID19098652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141074770..141398611hg38UCSC Ensembl
Innerchr2:141832339..142156180hg19UCSC Ensembl
Innerchr2:141548809..141872650hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38323842
hg19323842
hg18323842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729243
Samples
Known GenesLRP1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009434
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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