A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062357



Internal ID19151576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27579501hg38UCSC Ensembl
Innerchr19:27747981..28070409hg19UCSC Ensembl
Innerchr19:32439821..32762249hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38322429
hg19322429
hg18322429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3572016
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)nsv1062357
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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