A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851733



Internal ID22035376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7052252..7052252hg38UCSC Ensembl
chrY:6920293..6920293hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243076
Supporting Variants
Samples
Known GenesTBL1Y
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851733
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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