A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546063



Internal ID20919283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47397081..47397525hg38UCSC Ensembl
chr2:47624220..47624664hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258041
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546063
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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