A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564701



Internal ID20937772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2342383..2343138hg38UCSC Ensembl
chr7:2382018..2382773hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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