A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952760



Internal ID17301634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:129279006..129279905hg38UCSC Ensembl
Outerchr11:129148901..129149800hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999643
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952760
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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