A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134458



Internal ID18917647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63990284..63990353hg38UCSC Ensembl
Outerchr15:64282483..64282552hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971953
SamplesKWS2
Known GenesDAPK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134458
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