A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549168



Internal ID20922336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38987175..38988423hg38UCSC Ensembl
chr1:39452847..39454095hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381249
hg191249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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