A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540736



Internal ID20914026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37491301..37492198hg38UCSC Ensembl
chr1:37956902..37957799hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38898
hg19898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251069
Samples
Known GenesMEAF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540736
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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