A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953622



Internal ID16955809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54846646..54848845hg38UCSC Ensembl
Outerchr19:55358101..55360300hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999888
SamplesBILGI_BIOE
Known GenesKIR2DS4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953622
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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