A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1802n106



Internal ID20161159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50827242..50830642hg38UCSC Ensembl
chr19:51330498..51333898hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg383401
hg193401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121630, nsv1143907
SamplesKWS1
Known GenesKLK15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1802n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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