A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952700



Internal ID16954887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:132702797..132851596hg38UCSC Ensembl
Outerchr10:134516301..134665100hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38148800
hg19148800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998089
SamplesBILGI_BIOE
Known GenesINPP5A, NKX6-2, TTC40
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952700
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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