A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956339



Internal ID17305212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:99149173..99149454hg38UCSC Ensembl
Outerchr4:100070330..100070611hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004731
SamplesBILGI_BIOE
Known GenesLOC100507053
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956339
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