A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542946



Internal ID20916197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135223156..135223623hg38UCSC Ensembl
chr2:135980726..135981193hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255865
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542946
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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