A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537958



Internal ID20911285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37408438..39634613hg38UCSC Ensembl
chr3:37449929..39676104hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg382226176
hg192226176
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260005
Samples
Known GenesACAA1, ACVR2B, ACVR2B-AS1, C3orf35, CCR8, CSRNP1, CTDSPL, CX3CR1, DLEC1, EXOG, GORASP1, ITGA9, MIR26A1, MIR6822, MOBP, MYD88, OXSR1, PLCD1, RPSA, SCN10A, SCN11A, SCN5A, SLC22A13, SLC22A14, SLC25A38, SNORA6, SNORA62, TTC21A, VILL, WDR48, XIRP1, XYLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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