A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998951



Internal ID16945217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10291325..10295424hg38UCSC Ensembl
Outerchr19:10402001..10406100hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953974
Supporting Variants
SamplesBILGI_BIOE
Known GenesICAM5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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