A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562831



Internal ID20935902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142555219..148451915hg38UCSC Ensembl
chr3:142274061..148169702hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg385896697
hg195895642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262473
Samples
Known GenesATR, C3orf58, CHST2, LOC100289361, LOC100507389, PAQR9, PCOLCE2, PLOD2, PLS1, PLSCR1, PLSCR2, PLSCR4, PLSCR5, SLC9A9, SLC9A9-AS1, TRPC1, U2SURP, ZIC1, ZIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562831
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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