A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257992



Internal ID21400271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:25471426..25481429hg38UCSC Ensembl
chrY:27617573..27627576hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3810004
hg1910004
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730116
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257992
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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