A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248122



Internal ID20815162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150879988..150880255hg38UCSC Ensembl
chr1:150852464..150852731hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539251
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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