A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436706



Internal ID215315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:228018917..228027025hg38UCSC Ensembl
chr1:228206618..228214726hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg388109
hg198109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897489
Samples
Known GenesWNT3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436706
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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