A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539837



Internal ID20913132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40018654..40019008hg38UCSC Ensembl
chr1:40484326..40484680hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539837
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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