A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593663



Internal ID20966734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31382005..31384058hg38UCSC Ensembl
chr10:31670934..31672987hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228462
Samples
Known GenesZEB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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