A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971931



Internal ID18882651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41561637..41562545hg38UCSC Ensembl
Outerchr15:41853835..41854743hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134435
Supporting Variants
SamplesKWS2
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971931
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