A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540765



Internal ID20863742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171932647..171933296hg38UCSC Ensembl
chr2:172789157..172789806hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256086
Samples
Known GenesHAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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