A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951086



Internal ID17299960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:53199266..53202465hg38UCSC Ensembl
Outerchr13:53773401..53776600hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998224
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951086
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