A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150338



Internal ID15853379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32716739..32824007hg38UCSC Ensembl
Innerchr19:33207645..33314913hg19UCSC Ensembl
Innerchr19:37899485..38006753hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38107269
hg19107269
hg18107269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579314
Supporting Variants
Samples1780854128_A
Known GenesTDRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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