A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141385



Internal ID340581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164343000..164823324hg38UCSC Ensembl
chr5:163770006..164250330hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38480325
hg19480325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977543
Samples
Known GenesLOC101927835, LOC102546299
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141385
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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