A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562505



Internal ID335458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21170804..21170855hg38UCSC Ensembl
chrY:23332690..23332741hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562505
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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