A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549402



Internal ID20922564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9027345..9028563hg38UCSC Ensembl
chr2:9167474..9168692hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381219
hg191219
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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