A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275576



Internal ID20842616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:338944..467605hg38UCSC Ensembl
chr7:378910..507242hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38128662
hg19128333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567172
Supporting Variants
Samples
Known GenesLOC442497
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275576
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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