A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582808



Internal ID18881089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141045745..141276106hg38UCSC Ensembl
Innerchr2:141803314..142033675hg19UCSC Ensembl
Innerchr2:141519784..141750145hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38230362
hg19230362
hg18230362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003799
Supporting Variants
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)nssv3582808
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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