A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144834



Internal ID344039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64886235..64923990hg38UCSC Ensembl
chr17:62882353..62920108hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3837756
hg1937756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714099
Samples
Known GenesLRRC37A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144834
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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