A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999812



Internal ID16946078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:32719895..32721094hg38UCSC Ensembl
Outerchr19:33210801..33212000hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953276
Supporting Variants
SamplesBILGI_BIOE
Known GenesTDRD12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999812
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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