A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550596



Internal ID20923735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20493252..20494197hg38UCSC Ensembl
chr2:20693012..20693957hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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