A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276841



Internal ID20843881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87888694..87889781hg38UCSC Ensembl
chr7:87518009..87519096hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381088
hg191088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572644
Supporting Variants
Samples
Known GenesDBF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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