A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113831



Internal ID18937461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88603166..88603217hg38UCSC Ensembl
Outerchr16:88669574..88669625hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969908
SamplesKWS2
Known GenesZC3H18
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113831
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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