A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057762



Internal ID18800293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11804370..11950569hg38UCSC Ensembl
Innerchr19:11915185..12061384hg19UCSC Ensembl
Innerchr19:11776185..11922384hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38146200
hg19146200
hg18146200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3428n100
Supporting Variantsnssv3723284, nssv3564698, nssv3564697
Samples
Known GenesZNF439, ZNF440, ZNF491, ZNF69, ZNF700
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057762
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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