A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057408



Internal ID18799939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20646773..20746403hg38UCSC Ensembl
Innerchr19:20829579..20929209hg19UCSC Ensembl
Innerchr19:20621419..20721049hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3899631
hg1999631
hg1899631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3468n100
Supporting Variantsnssv3570550
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)nsv1057408
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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