A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272188



Internal ID20839228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103328096..103328473hg38UCSC Ensembl
chr7:102968543..102968920hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564771
Supporting Variants
Samples
Known GenesDNAJC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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