A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951852



Internal ID17300726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:115582091..115588090hg38UCSC Ensembl
Outerchr10:117341601..117347600hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998052
SamplesBILGI_BIOE
Known GenesATRNL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951852
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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