A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538681



Internal ID20911995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26405850..26406444hg38UCSC Ensembl
chr2:26628718..26629312hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257535
Samples
Known GenesDRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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