A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275679



Internal ID20842719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68467628..68501553hg38UCSC Ensembl
chr7:67932615..67966540hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3833926
hg1933926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275679
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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