A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131094



Internal ID18928166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83284348..83284748hg38UCSC Ensembl
Outerchr15:83953100..83953500hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1257n106
Supporting Variantsnssv3967800
SamplesKWS2
Known GenesBNC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131094
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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