A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536176



Internal ID311716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7065096..7065885hg38UCSC Ensembl
chrY:6933137..6933926hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738311
Samples
Known GenesTBL1Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536176
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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