A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548708



Internal ID20921891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240589403..240590422hg38UCSC Ensembl
chr1:240752703..240753722hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250110
Samples
Known GenesGREM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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