A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256503



Internal ID21398811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17951261..17954718hg38UCSC Ensembl
chrY:20063141..20066598hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg383458
hg193458
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730265
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256503
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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