A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951877



Internal ID17300751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:128457337..128464336hg38UCSC Ensembl
Outerchr10:130255601..130262600hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998075
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951877
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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