A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563766



Internal ID20936837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14052897..14065310hg38UCSC Ensembl
chr7:14092522..14104935hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3812414
hg1912414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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