A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258103



Internal ID21400301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:16269426..16322813hg38UCSC Ensembl
chrY:18381306..18434693hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3853388
hg1953388
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730052
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258103
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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