A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952424



Internal ID16954611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:19033592..19069091hg38UCSC Ensembl
Outerchr19:19144401..19179900hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3835500
hg1935500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998974
SamplesBILGI_BIOE
Known GenesARMC6, SLC25A42
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952424
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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