A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981471



Internal ID19208909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29494293..29494993hg38UCSC Ensembl
Outerchr19:29985200..29985900hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121974
Supporting Variants
SamplesKWS1
Known GenesLOC284395
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981471
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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