A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526129



Internal ID20899490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48935443..48938014hg38UCSC Ensembl
chr18:46461813..46464384hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg382572
hg192572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042103
Samples
Known GenesSMAD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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