A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275125



Internal ID20842165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94895505..94895817hg38UCSC Ensembl
chr7:94524817..94525129hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275125
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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