A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013201



Internal ID19102419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:53246288..53326246hg38UCSC Ensembl
Innerchr2:53473426..53553384hg19UCSC Ensembl
Innerchr2:53326930..53406888hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3879959
hg1979959
hg1879959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576620
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)nsv1013201
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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