A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952703



Internal ID16954890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133037897..133143896hg38UCSC Ensembl
Outerchr10:134851401..134957400hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38106000
hg19106000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998092
SamplesBILGI_BIOE
Known GenesGPR123
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952703
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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