A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257444



Internal ID21400495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179634372..179655065hg38UCSC Ensembl
chr5:179061373..179082066hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3820694
hg1920694
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730180
Supporting Variants
SamplesNA19239
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257444
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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