A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624380



Internal ID21572685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1681966..1681966hg38UCSC Ensembl
chrY:1750859..1750859hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169949, nssv17169948
SamplesHG03125, HG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624380
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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