A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549484



Internal ID20922645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207593276..207593740hg38UCSC Ensembl
chr2:208458000..208458464hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4272n223
Supporting Variantsnssv18258554
Samples
Known GenesCREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549484
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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