A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730158



Internal ID21400969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:24762481..24889160hg38UCSC Ensembl
chrY:26908628..27035307hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38126680
hg19126680
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257542
SamplesNA19239
Known GenesDAZ2, DAZ3, DAZ4
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730158
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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