A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528986



Internal ID20902347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24391968..24393565hg38UCSC Ensembl
chr18:21971932..21973529hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039474
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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