A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275604



Internal ID20842644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35829129..35830217hg38UCSC Ensembl
chr7:35868739..35869827hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg381089
hg191089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561452
Supporting Variants
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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