A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111934



Internal ID19285936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90858866..90859186hg38UCSC Ensembl
Outerchr15:91402096..91402416hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1260n106
Supporting Variantsnssv3970993, nssv3966280
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111934
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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