A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590513



Internal ID20963584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73164285..73164513hg38UCSC Ensembl
chr10:74924043..74924271hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234020
Samples
Known GenesECD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590513
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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