A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258624



Internal ID21399070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20060965..20083032hg38UCSC Ensembl
chrY:22222851..22244918hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3822068
hg1922068
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730145
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258624
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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