A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540400



Internal ID20913691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45031151..45031778hg38UCSC Ensembl
chr1:45496823..45497450hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251873
Samples
Known GenesZSWIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540400
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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