A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582725



Internal ID20955796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114052901..114053388hg38UCSC Ensembl
chr10:115812660..115813147hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221347
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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