A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545877



Internal ID20919101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224530882..224531357hg38UCSC Ensembl
chr2:225395599..225396074hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257140
Samples
Known GenesCUL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545877
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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