A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574634



Internal ID20947705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185622818..185623831hg38UCSC Ensembl
chr3:185340606..185341619hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg381014
hg191014
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261228
Samples
Known GenesSENP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574634
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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