A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532926



Internal ID20906287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29502366..29503049hg38UCSC Ensembl
chr18:27082331..27083014hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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