A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063535



Internal ID19152754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19695577..19752822hg38UCSC Ensembl
Innerchr19:19806386..19863631hg19UCSC Ensembl
Innerchr19:19667386..19724631hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3857246
hg1957246
hg1857246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3455n100
Supporting Variantsnssv3569787
Samples
Known GenesZNF14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063535
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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