A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126437



Internal ID18906717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:83968195..83968895hg38UCSC Ensembl
Outerchr16:84001800..84002500hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984685
SamplesKWS1
Known GenesNECAB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126437
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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