A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549258



Internal ID20922426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238107922..238108875hg38UCSC Ensembl
chr1:238271222..238272175hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n223
Supporting Variantsnssv18251425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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