A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953939



Internal ID16956126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:1104902..1174301hg38UCSC Ensembl
Outerchr19:1104901..1174300hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3869400
hg1969400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998918
SamplesBILGI_BIOE
Known GenesGPX4, SBNO2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953939
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer