A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256894



Internal ID21399232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179636890..179655737hg38UCSC Ensembl
chr5:179063891..179082738hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3818848
hg1918848
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730180
Supporting Variants
SamplesHG00732
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256894
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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