A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138455



Internal ID19271594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:54653484..54653559hg38UCSC Ensembl
Outerchr16:54687396..54687471hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991027
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138455
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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