A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671877



Internal ID21620184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9613625..9614159hg38UCSC Ensembl
chrY:9451234..9451768hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170965
SamplesHG02492
Known GenesRBMY3AP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671877
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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