A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138218



Internal ID337401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12509925..12520385hg38UCSC Ensembl
chrY:14621727..14632316hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3810461
hg1910590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138218
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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