A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576367



Internal ID20949438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1492128..3536924hg38UCSC Ensembl
chr10:1534323..3579116hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg382044797
hg192044794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218595
Samples
Known GenesADARB2, ADARB2-AS1, LINC00700, LINC00701, MIR6072, PFKP, PITRM1, PITRM1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576367
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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