A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272201



Internal ID20839241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103844126..103847747hg38UCSC Ensembl
chr7:103484573..103488194hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383622
hg193622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564714
Supporting Variants
Samples
Known GenesRELN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272201
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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