A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981477



Internal ID19208660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:46648943..46649643hg38UCSC Ensembl
Outerchr19:47152200..47152900hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144876
Supporting Variants
SamplesKWS1
Known GenesDACT3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981477
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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