A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668498



Internal ID21616803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2597263..2598377hg38UCSC Ensembl
chrY:2465304..2466418hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381115
hg191115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170609
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668498
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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