A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504544



Internal ID20877806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20790830..20792631hg38UCSC Ensembl
chr16:20802152..20803953hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028810
Samples
Known GenesACSM3, ERI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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