A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975091



Internal ID22750026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20260212..20445457hg38UCSC Ensembl
chrY:22422098..22607343hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38185246
hg19185246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466189
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975091
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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