A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968274



Internal ID18859316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:50827242..50830636hg38UCSC Ensembl
Outerchr19:51330498..51333892hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg383395
hg193395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121630
Supporting Variants
SamplesKWS1
Known GenesKLK15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968274
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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