A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730265



Internal ID21401076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17951224..18012034hg38UCSC Ensembl
chrY:20063104..20123914hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3860811
hg1960811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16255879, nssv16256503, nssv16258444
SamplesHG00512, NA19239, HG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730265
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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