A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553331



Internal ID20926439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49253853..49255084hg38UCSC Ensembl
chr3:49291286..49292517hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262809
Samples
Known GenesCCDC36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553331
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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