A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536584



Internal ID20909930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:108793247..108793527hg38UCSC Ensembl
chr2:109409703..109409983hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256460
Samples
Known GenesCCDC138
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536584
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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