A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999886



Internal ID16946152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54832146..54835845hg38UCSC Ensembl
Outerchr19:55343601..55347300hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953620
Supporting Variants
SamplesBILGI_BIOE
Known GenesKIR2DS4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999886
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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