A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608013



Internal ID21556318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1564609..1564609hg38UCSC Ensembl
chrY:1633502..1633502hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169642
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608013
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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