A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064400



Internal ID19153619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19990243..20614318hg38UCSC Ensembl
Innerchr19:20101052..20797124hg19UCSC Ensembl
Innerchr19:19962052..20588964hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38624076
hg19696073
hg18626913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3457n100
Supporting Variantsnssv3569796
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)nsv1064400
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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