A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256674



Internal ID21397824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179636868..179655106hg38UCSC Ensembl
chr5:179063869..179082107hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3818239
hg1918239
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730180
Supporting Variants
SamplesHG00512
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256674
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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