A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136289



Internal ID18929729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54844845..54855145hg38UCSC Ensembl
Outerchr19:55356300..55366600hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3810301
hg1910301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989906
SamplesKWS2
Known GenesKIR2DS4, KIR3DL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136289
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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