A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275789



Internal ID20842829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98001407..98002127hg38UCSC Ensembl
chr7:97630719..97631439hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275789
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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