A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567047



Internal ID20940118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3141363..3141958hg38UCSC Ensembl
chr7:3180997..3181592hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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