A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579885



Internal ID20952956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15743181..15760248hg38UCSC Ensembl
chr10:15785180..15802247hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817068
hg1917068
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv616n223
Supporting Variantsnssv18231635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579885
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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