A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276829



Internal ID20843869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87094471..87149103hg38UCSC Ensembl
chr7:86723787..86778419hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3854633
hg1954633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566080
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276829
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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