A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577524



Internal ID20950595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102325369..102325913hg38UCSC Ensembl
chr10:104085126..104085670hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233581
Samples
Known GenesGBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577524
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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