A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559801



Internal ID20932872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135993808..135994389hg38UCSC Ensembl
chr7:135678556..135679137hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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