A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248280



Internal ID20815320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200676369..200677313hg38UCSC Ensembl
chr1:200645497..200646441hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248280
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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