A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138800



Internal ID337984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7892272..8147953hg38UCSC Ensembl
chrY:7760313..8015994hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38255682
hg19255682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138800
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer