A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587131



Internal ID20960202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97472863..97474084hg38UCSC Ensembl
chr10:99232620..99233841hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv866n223
Supporting Variantsnssv18228768
Samples
Known GenesMMS19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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