A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998662



Internal ID19158198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49308617..49497641hg38UCSC Ensembl
Innerchr2:49535756..49724779hg19UCSC Ensembl
Innerchr2:49389260..49578283hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38189025
hg19189024
hg18189024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726009
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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