A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951864



Internal ID17300738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122199986..122205585hg38UCSC Ensembl
Outerchr10:123959501..123965100hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998063
SamplesBILGI_BIOE
Known GenesTACC2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951864
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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