A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549820



Internal ID20922971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86561431..86562224hg38UCSC Ensembl
chr2:86788554..86789347hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260927
Samples
Known GenesCHMP3, RNF103-CHMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549820
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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