A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138820



Internal ID338004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:523968..529968hg38UCSC Ensembl
chr5:180715774..180721464hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386001
hg195691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2n206
Supporting Variantsnssv16896940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138820
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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