A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539263



Internal ID20912564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215389145..215389685hg38UCSC Ensembl
chr2:216253868..216254408hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258683
Samples
Known GenesFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539263
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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