A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543860



Internal ID20917101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67900580..67901302hg38UCSC Ensembl
chr1:68366263..68366985hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251291
Samples
Known GenesGNG12-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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