A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247993



Internal ID20815033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164701696..165001499hg38UCSC Ensembl
chr1:164670933..164970736hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38299804
hg19299804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542090
Supporting Variants
Samples
Known GenesLOC100505795, PBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247993
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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