A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538201



Internal ID20911524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8298598..8299112hg38UCSC Ensembl
chr1:8358658..8359172hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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