A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549352



Internal ID20922514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216085865..216086363hg38UCSC Ensembl
chr2:216950588..216951086hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259296
Samples
Known GenesTMEM169
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549352
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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