A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572479



Internal ID20945550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43751413..43751895hg38UCSC Ensembl
chr7:43791012..43791494hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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