A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274179



Internal ID20841219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6464198..6465301hg38UCSC Ensembl
chr7:6503829..6504932hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572564
Supporting Variants
Samples
Known GenesKDELR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274179
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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