A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067189



Internal ID18809720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32712741..32816579hg38UCSC Ensembl
Innerchr19:33203647..33307485hg19UCSC Ensembl
Innerchr19:37895487..37999325hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38103839
hg19103839
hg18103839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566574
Samples
Known GenesNUDT19, TDRD12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067189
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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