A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067199



Internal ID18809730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57622557..57643587hg38UCSC Ensembl
Innerchr19:58133925..58154955hg19UCSC Ensembl
Innerchr19:62825737..62846767hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3821031
hg1921031
hg1821031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3685n100
Supporting Variantsnssv3726650
Samples
Known GenesZNF211
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067199
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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