A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111517



Internal ID19263644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90858833..90859195hg38UCSC Ensembl
Outerchr15:91402063..91402425hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1260n106
Supporting Variantsnssv3963653
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111517
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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