A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949813



Internal ID17298687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:119993246..119999945hg38UCSC Ensembl
Outerchr4:120914401..120921100hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996773
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949813
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