A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055327



Internal ID19144546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57479132..57492505hg38UCSC Ensembl
Innerchr19:57990500..58003873hg19UCSC Ensembl
Innerchr19:62682312..62695685hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3813374
hg1913374
hg1813374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3684n100
Supporting Variantsnssv3570452, nssv3570451
Samples
Known GenesZNF419
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055327
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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