A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965511



Internal ID18898433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41573468..41573712hg38UCSC Ensembl
Outerchr15:41865666..41865910hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121509
Supporting Variants
SamplesKWS2
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965511
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