A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984786



Internal ID18869775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54839945..54859745hg38UCSC Ensembl
Outerchr19:55351400..55371200hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819801
hg1919801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126532
Supporting Variants
SamplesKWS1
Known GenesKIR2DS4, KIR3DL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984786
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