A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109037



Internal ID18915862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89448142..89448196hg38UCSC Ensembl
Outerchr16:89514550..89514604hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954871
SamplesKWS1
Known GenesANKRD11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109037
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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