A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135854



Internal ID18939742
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 StatusM
Merged Variants
Supporting Variantsnssv3989448
SamplesKWS2
Known GenesKIR2DS4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135854
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer