A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567564



Internal ID20940635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21737806..21739254hg38UCSC Ensembl
chr7:21777424..21778872hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272652
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567564
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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