A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577686



Internal ID20950757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102551086..102551740hg38UCSC Ensembl
chr10:104310843..104311497hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234710
Samples
Known GenesSUFU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577686
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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