A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958510



Internal ID17307383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14894363..14894611hg38UCSC Ensembl
Outerchr10:14936362..14936610hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004877
SamplesBILGI_BIOE
Known GenesSUV39H2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958510
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