A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257468



Internal ID21400501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15876622..15904760hg38UCSC Ensembl
chrY:17988502..18016640hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3828139
hg1928139
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730215
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257468
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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