A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590075



Internal ID20963146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21468560..21470082hg38UCSC Ensembl
chr10:21757489..21759011hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381523
hg191523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590075
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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