A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257678



Internal ID21398321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179637006..179656672hg38UCSC Ensembl
chr5:179064007..179083673hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3819667
hg1919667
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730180
Supporting Variants
SamplesHG00513
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257678
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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