A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256877



Internal ID21398052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21021401..21051594hg38UCSC Ensembl
chrY:23183287..23213480hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3830194
hg1930194
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730075
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256877
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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