A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584802



Internal ID20957873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9292743..9293502hg38UCSC Ensembl
chr10:9334706..9335465hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584802
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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