A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580074



Internal ID20953145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119507609..119509425hg38UCSC Ensembl
chr10:121267121..121268937hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv899n223
Supporting Variantsnssv18232093
Samples
Known GenesRGS10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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