A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549762



Internal ID20922917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213943430..213946409hg38UCSC Ensembl
chr2:214808154..214811133hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg382980
hg192980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258653
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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