A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503532



Internal ID20876787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20334036..20334602hg38UCSC Ensembl
chr16:20345358..20345924hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028368
Samples
Known GenesUMOD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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