A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566984



Internal ID20940055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95627447..95628154hg38UCSC Ensembl
chr7:95256759..95257466hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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