A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552233



Internal ID20925361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207240038..207240907hg38UCSC Ensembl
chr1:207413383..207414252hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552233
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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