A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587832



Internal ID20960903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97472410..97474027hg38UCSC Ensembl
chr10:99232167..99233784hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381618
hg191618
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv866n223
Supporting Variantsnssv18231591
Samples
Known GenesMMS19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587832
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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