A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553419



Internal ID20926527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215277587..215278511hg38UCSC Ensembl
chr2:216142310..216143234hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4280n223
Supporting Variantsnssv18258677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553419
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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