A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969018



Internal ID18895947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54789948..54818945hg38UCSC Ensembl
Outerchr19:55301400..55330400hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3828998
hg1929001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133456
Supporting Variants
SamplesKWS2
Known GenesKIR2DL4, KIR3DL1, LOC100287534
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969018
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