A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256729



Internal ID21399660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63835828..63844108hg38UCSC Ensembl
chr9:68431562..68439842hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg388281
hg198281
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesHG00733
Known GenesLOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256729
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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