A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594603



Internal ID20967674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92515312..92515989hg38UCSC Ensembl
chr10:94275069..94275746hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230442
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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