A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566952



Internal ID20940023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:115856809..115857552hg38UCSC Ensembl
chr7:115496863..115497606hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274339
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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