A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257909



Internal ID21397953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9817206..9914577hg38UCSC Ensembl
chrY:9654815..9752186hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3897372
hg1997372
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730219
Supporting Variants
SamplesHG00512
Known GenesTTTY23, TTTY23B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257909
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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