A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999235



Internal ID19158771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82553793..82648187hg38UCSC Ensembl
Innerchr1:83019476..83113870hg19UCSC Ensembl
Innerchr1:82792064..82886458hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3894395
hg1994395
hg1894395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3699594
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)nsv999235
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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