A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262945



Internal ID20829985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74002927..74003733hg38UCSC Ensembl
chr3:74052078..74052884hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262945
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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