A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060950



Internal ID19150169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12395059..12431081hg38UCSC Ensembl
Innerchr19:12505873..12541895hg19UCSC Ensembl
Innerchr19:12366873..12402895hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3836023
hg1936023
hg1836023
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3432n100
Supporting Variantsnssv3564710, nssv3723286, nssv3723287, nssv3564709, nssv3723285
Samples
Known GenesZNF443, ZNF799
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060950
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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