A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539668



Internal ID20912964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161317715..161318096hg38UCSC Ensembl
chr1:161287505..161287886hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247347
Samples
Known GenesSDHC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539668
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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