A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730232



Internal ID21401043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:24180042..24250285hg38UCSC Ensembl
chrY:26326189..26396432hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3870244
hg1970244
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257399, nssv16256263
SamplesHG00512
Known GenesCSPG4P1Y, GOLGA2P2Y, GOLGA2P3Y
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730232
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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