A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567935



Internal ID20941006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130335846..130336531hg38UCSC Ensembl
chr7:129975686..129976371hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567935
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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