A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952754



Internal ID16954941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125070905..125093704hg38UCSC Ensembl
Outerchr11:124940801..124963600hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3822800
hg1922800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999637
SamplesBILGI_BIOE
Known GenesSLC37A2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952754
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