A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259604



Internal ID20826644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128972246..128972870hg38UCSC Ensembl
chr3:128691089..128691713hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558476
Supporting Variants
Samples
Known GenesKIAA1257
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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