A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439985



Internal ID218509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33129839..33130783hg38UCSC Ensembl
chr3:33171331..33172275hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932416
Samples
Known GenesCRTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439985
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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