A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540174



Internal ID20913466
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 StatusM
Merged Variants
Supporting Variantsnssv18262945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540174
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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