A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134435



Internal ID18928005
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 StatusM
Merged Variantsdgv1196n106
Supporting Variantsnssv3971931, nssv3964800
SamplesKWS2, KWS1
Known GenesTYRO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134435
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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