A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140511



Internal ID339704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168564067..168566012hg38UCSC Ensembl
chr5:167991072..167993017hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381946
hg191946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976616
Samples
Known GenesPANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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