A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434997



Internal ID213657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183548786..183549182hg38UCSC Ensembl
chr3:183266574..183266970hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944745
Samples
Known GenesKLHL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434997
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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