A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956916



Internal ID16959103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131916882..131918759hg38UCSC Ensembl
Outerchr10:133730386..133732263hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001954
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956916
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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