A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552650



Internal ID20925776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65444313..65444959hg38UCSC Ensembl
chr2:65671447..65672093hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552650
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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