A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730162



Internal ID21400973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18640415..18733657hg38UCSC Ensembl
chrY:20802301..20895543hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3893243
hg1993243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257103, nssv16257847
SamplesHG00512
Known GenesHSFY1, HSFY2, TTTY9A, TTTY9B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730162
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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