A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562078



Internal ID20935149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79642457..79642983hg38UCSC Ensembl
chr7:79271773..79272299hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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