A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951857



Internal ID16954044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:117534490..117543789hg38UCSC Ensembl
Outerchr10:119294001..119303300hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998057
SamplesBILGI_BIOE
Known GenesEMX2, EMX2OS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951857
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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