A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255977



Internal ID21399840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63839177..63842903hg38UCSC Ensembl
chr9:68434911..68438637hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg383727
hg193727
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesNA19238
Known GenesLOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255977
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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