A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275813



Internal ID20842853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98428592..98429104hg38UCSC Ensembl
chr7:98057904..98058416hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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