A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153981



Internal ID18854410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54804375..54811604hg38UCSC Ensembl
Outerchr19:55315830..55323059hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg387230
hg197230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003251
SamplesKWB1
Known GenesKIR2DL4, LOC100287534
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153981
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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