A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545926



Internal ID20919150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31870671..31871887hg38UCSC Ensembl
chr2:32095740..32096956hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260038
Samples
Known GenesMEMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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