A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272187



Internal ID20839227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103325438..103326278hg38UCSC Ensembl
chr7:102965885..102966725hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572233
Supporting Variants
Samples
Known GenesDNAJC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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