A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952707



Internal ID17301581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133333097..133403896hg38UCSC Ensembl
Outerchr10:135146601..135217400hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3870800
hg1970800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998096
SamplesBILGI_BIOE
Known GenesCALY, ECHS1, FUOM, MIR3944, MTG1, PAOX, PRAP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952707
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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