A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999880



Internal ID19159416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:78801696..78901579hg38UCSC Ensembl
Innerchr2:79028822..79128705hg19UCSC Ensembl
Innerchr2:78882330..78982213hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3899884
hg1999884
hg1899884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582111
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)nsv999880
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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