A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503264



Internal ID20876517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75643932..75645769hg38UCSC Ensembl
chr16:75677830..75679667hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381838
hg191838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032730
Samples
Known GenesKARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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