A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564192



Internal ID20937263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24445739..24446022hg38UCSC Ensembl
chr7:24485358..24485641hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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