A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578311



Internal ID20951382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9857689..9858810hg38UCSC Ensembl
chr12:10010288..10011409hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219003
Samples
Known GenesCLEC2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578311
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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