A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556292



Internal ID20929363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185626583..185627597hg38UCSC Ensembl
chr3:185344371..185345385hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261229
Samples
Known GenesSENP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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