A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622828



Internal ID21571133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7720499..7720499hg38UCSC Ensembl
chrY:7588540..7588540hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383325
hg193325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170917
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622828
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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