A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256538



Internal ID21400314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20062841..20085126hg38UCSC Ensembl
chrY:22224727..22247012hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3822286
hg1922286
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730145
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256538
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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