A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258592



Internal ID20825632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208558486..208559068hg38UCSC Ensembl
chr2:209423211..209423793hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258592
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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