A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258444



Internal ID21400399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17951224..18012034hg38UCSC Ensembl
chrY:20063104..20123914hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3860811
hg1960811
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730265
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258444
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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