A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248128



Internal ID20815168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150939252..150940442hg38UCSC Ensembl
chr1:150911728..150912918hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550013
Supporting Variants
Samples
Known GenesSETDB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248128
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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