A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055694



Internal ID19144913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19978057..20619795hg38UCSC Ensembl
Innerchr19:20088866..20802601hg19UCSC Ensembl
Innerchr19:19949866..20594441hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38641739
hg19713736
hg18644576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3457n100
Supporting Variantsnssv3569794
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055694
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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