A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002837



Internal ID16949103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54755167..54769949hg38UCSC Ensembl
Outerchr19:55266619..55281401hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3814783
hg1914783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956586
Supporting Variants
SamplesBILGI_BIOE
Known GenesKIR2DL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002837
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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