A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547709



Internal ID20920910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161543821..161544448hg38UCSC Ensembl
chr2:162400331..162400958hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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