A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968553



Internal ID19226564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24871653..24873553hg38UCSC Ensembl
Outerchr15:25116800..25118700hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121891
Supporting Variants
SamplesKWS2
Known GenesSNRPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968553
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