A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548307



Internal ID20921499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:48257960..48258358hg38UCSC Ensembl
chr2:48485099..48485497hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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