A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551375



Internal ID324838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76851082..76851082hg38UCSC Ensembl
chr18:74563038..74563038hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719654
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551375
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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