A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531561



Internal ID20904922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22979077..23102440hg38UCSC Ensembl
chr18:20559040..20682404hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38123364
hg19123365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040347
Samples
Known GenesRBBP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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