A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546730



Internal ID20919940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31632768..31651238hg38UCSC Ensembl
chr2:31857837..31876307hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3818471
hg1918471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546730
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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