A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055911



Internal ID18798442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20653072..20794520hg38UCSC Ensembl
Innerchr19:20835878..20977326hg19UCSC Ensembl
Innerchr19:20627718..20769166hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38141449
hg19141449
hg18141449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3467n100
Supporting Variantsnssv3570567, nssv3570566
Samples
Known GenesZNF626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055911
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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