A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565914



Internal ID20938985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14058549..14075041hg38UCSC Ensembl
chr7:14098174..14114666hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3816493
hg1916493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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