A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003802



Internal ID18746333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20057935..20154347hg38UCSC Ensembl
Innerchr1:20384428..20480840hg19UCSC Ensembl
Innerchr1:20257015..20353427hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3896413
hg1996413
hg1896413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3700851
Samples
Known GenesPLA2G2D, PLA2G2F, PLA2G5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003802
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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