A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188139



Internal ID20755179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86336528..86433745hg38UCSC Ensembl
chr16:86370134..86467351hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3897218
hg1997218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499069
Supporting Variants
Samples
Known GenesLINC00917
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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