A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576417



Internal ID20949488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72346984..72347865hg38UCSC Ensembl
chr10:74106742..74107623hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217768
Samples
Known GenesDNAJB12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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