A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528877



Internal ID20902238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25563157..25563833hg38UCSC Ensembl
chr20:25543793..25544469hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067176
Samples
Known GenesNINL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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