A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256161



Internal ID21398102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:16254055..16315867hg38UCSC Ensembl
chrY:18365935..18427747hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3861813
hg1961813
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730052
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256161
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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