A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255982



Internal ID21400618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61817864..61927345hg38UCSC Ensembl
chr9:44958294..45063497hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38109482
hg19105204
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730187
Supporting Variants
SamplesNA19240
Known GenesFAM27C
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255982
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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