A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555019



Internal ID20928108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38521170..38522368hg38UCSC Ensembl
chr1:38986842..38988040hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252411
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555019
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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