A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513750



Internal ID20887097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85068657..85218092hg38UCSC Ensembl
chr16:85102263..85251698hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38149436
hg19149436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183271
Samples
Known GenesFAM92B, KIAA0513, LOC400548
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513750
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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