A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507942



Internal ID20881238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80920201..80965600hg38UCSC Ensembl
chr16:80954098..80999497hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3845400
hg1945400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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