A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554934



Internal ID20928024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33386095..33386465hg38UCSC Ensembl
chr1:33851696..33852066hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv155n223
Supporting Variantsnssv18250885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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