A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989880



Internal ID19243458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1789801..1790701hg38UCSC Ensembl
Outerchr19:1789800..1790700hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112736
Supporting Variants
SamplesKWS2
Known GenesATP8B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989880
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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