A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256263



Internal ID21397891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:24188679..24250285hg38UCSC Ensembl
chrY:26334826..26396432hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3861607
hg1961607
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730232
Supporting Variants
SamplesHG00512
Known GenesGOLGA2P2Y, GOLGA2P3Y
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256263
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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