A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989448



Internal ID18898051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54833506..54834441hg38UCSC Ensembl
Outerchr19:55344961..55345896hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38936
hg19936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135854
Supporting Variants
SamplesKWS2
Known GenesKIR2DS4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989448
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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