A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769024



Internal ID18964966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54716700..54817245hg38UCSC Ensembl
chr19:55228199..55328700hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38100546
hg19100502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071948
Supporting Variants
SamplesKWP1
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR3DL1, KIR3DL3, LOC100287534
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769024
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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