A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623057



Internal ID21571362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:527097..527097hg38UCSC Ensembl
chrY:437832..437832hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg383281
hg193281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170834
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623057
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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