A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591593



Internal ID20964664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9479972..9510053hg38UCSC Ensembl
chr10:9521935..9552016hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3830082
hg1930082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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