A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957899



Internal ID16960086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:124960172..124960322hg38UCSC Ensembl
Outerchr11:124830068..124830218hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002642
SamplesBILGI_BIOE
Known GenesCCDC15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957899
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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