A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568395



Internal ID20941466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67911588..67912433hg38UCSC Ensembl
chr7:67376575..67377420hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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