A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983150



Internal ID19204172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36351575..36351691hg38UCSC Ensembl
Outerchr11:36373125..36373241hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145515
Supporting Variants
SamplesKWS1
Known GenesPRR5L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983150
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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