A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548340



Internal ID20921527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200011474..200013587hg38UCSC Ensembl
chr1:199980602..199982715hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382114
hg192114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv508n223
Supporting Variantsnssv18248237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548340
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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