A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545505



Internal ID20918735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47627183..47628723hg38UCSC Ensembl
chr2:47854322..47855862hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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