A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532246



Internal ID20905607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33577201..33579100hg38UCSC Ensembl
chr18:31157165..31159064hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041244
Samples
Known GenesASXL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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