A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548241



Internal ID20921437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70318702..70319619hg38UCSC Ensembl
chr1:70784385..70785302hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251341
Samples
Known GenesANKRD13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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