A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554087



Internal ID20927196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164466625..164467666hg38UCSC Ensembl
chr2:165323135..165324176hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4174n223
Supporting Variantsnssv18255811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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