A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064177



Internal ID19153396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27659768hg38UCSC Ensembl
Innerchr19:27747981..28150676hg19UCSC Ensembl
Innerchr19:32439821..32842516hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38402696
hg19402696
hg18402696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3499n100
Supporting Variantsnssv3572032
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)nsv1064177
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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