A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144756



Internal ID18934698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:11668344..11668644hg38UCSC Ensembl
Outerchr16:11762200..11762500hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981348
SamplesKWS1
Known GenesSNN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144756
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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