A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503562



Internal ID20876817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74719502..74723056hg38UCSC Ensembl
chr16:74753400..74756954hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg383555
hg193555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031435
Samples
Known GenesFA2H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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