A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531058



Internal ID20904419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25124601..25125500hg38UCSC Ensembl
chr18:22704565..22705464hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039519
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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