A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583199



Internal ID20956270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72225630..72226155hg38UCSC Ensembl
chr10:73985388..73985913hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229433
Samples
Known GenesANAPC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583199
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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