A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669484



Internal ID21617790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56827926..56828110hg38UCSC Ensembl
chrY:58974073..58974257hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170880
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669484
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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