A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499069



Internal ID20872285
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 StatusM
Merged Variants
Supporting Variantsnssv18188139
Samples
Known GenesLINC00917
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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