A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273367



Internal ID20840407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26427254..26427696hg38UCSC Ensembl
chr7:26466874..26467316hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556826
Supporting Variants
Samples
Known GenesLOC441204
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273367
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00027


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