A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951868



Internal ID17300742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:124864132..124867831hg38UCSC Ensembl
Outerchr10:126552701..126556400hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998067
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951868
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