A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257511



Internal ID21398796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41309929..41573547hg38UCSC Ensembl
chr9:67864602..70690704hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38263619
hg192826103
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730044
Supporting Variants
SamplesHG00514
Known GenesANKRD20A1, ANKRD20A3, ANKRD20A4, CBWD3, CBWD5, CBWD6, FOXD4L2, FOXD4L4, FOXD4L5, FOXD4L6, LOC100132352, LOC100133920, LOC440896, LOC642236, PGM5P2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257511
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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