A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561440



Internal ID20934511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113930500..113931564hg38UCSC Ensembl
chr7:113570555..113571619hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561440
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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