A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669603



Internal ID21617908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56825979..56826038hg38UCSC Ensembl
chrY:58972126..58972185hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170878
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669603
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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