A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541023



Internal ID20914308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171454163..171454421hg38UCSC Ensembl
chr2:172310673..172310931hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256062
Samples
Known GenesDCAF17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541023
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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