A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586571



Internal ID20959642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21018201..21018807hg38UCSC Ensembl
chr10:21307130..21307736hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233365
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586571
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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