A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138989



Internal ID338173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14022623..14180818hg38UCSC Ensembl
chrY:16134503..16292698hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38158196
hg19158196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738434
Samples
Known GenesVCY, VCY1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138989
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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