A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952460



Internal ID17301334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:62127329..62154428hg38UCSC Ensembl
Outerchr11:61894801..61921900hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3827100
hg1927100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999555
SamplesBILGI_BIOE
Known GenesINCENP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952460
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer