A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566574



Internal ID18518169
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 StatusS
Merged Variantsnsv1067189
Supporting Variants
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)nssv3566574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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