A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539777



Internal ID20913072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172914353..172915721hg38UCSC Ensembl
chr2:173779081..173780449hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256113
Samples
Known GenesRAPGEF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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