A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539689



Internal ID20912984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220764185..220764747hg38UCSC Ensembl
chr1:220937527..220938089hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249281
Samples
Known GenesMARC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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