A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730088



Internal ID21400904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18172892..18292282hg38UCSC Ensembl
chrY:20334778..20454168hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38119391
hg19119391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257026
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730088
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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