A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969400



Internal ID18890597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:33194194..33194894hg38UCSC Ensembl
Outerchr19:33685100..33685800hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121977
Supporting Variants
SamplesKWS2
Known GenesLRP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969400
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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