A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257145



Internal ID21397811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:25930350..26116417hg38UCSC Ensembl
chrY:28076497..28262564hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38186068
hg19186068
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730275
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257145
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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