A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272193



Internal ID20839233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103528535..103529066hg38UCSC Ensembl
chr7:103168982..103169513hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563305
Supporting Variants
Samples
Known GenesRELN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272193
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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