A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570858



Internal ID20943929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155400955..155406153hg38UCSC Ensembl
chr3:155118744..155123942hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg385199
hg195199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570858
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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