A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526156



Internal ID302295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31526326..31526431hg38UCSC Ensembl
chr18:29106289..29106394hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717074
Samples
Known GenesDSG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526156
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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