A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249997



Internal ID20817037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206132954..206133455hg38UCSC Ensembl
chr1:206207876..206208377hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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