A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546799



Internal ID20920009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56562825..56563155hg38UCSC Ensembl
chr3:56596853..56597183hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261485
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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