A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260386



Internal ID20827426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15516882..15517981hg38UCSC Ensembl
chr3:15558389..15559488hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554196
Supporting Variants
Samples
Known GenesCOLQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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