A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275115



Internal ID20842155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94711671..94713472hg38UCSC Ensembl
chr7:94340983..94342784hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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