A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672210



Internal ID21620515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179633843..179658554hg38UCSC Ensembl
chr5:179060844..179085555hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3824712
hg1924712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123584
Samples
Known GenesC5orf60
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672210
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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