A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574614



Internal ID20947685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135775579..135776388hg38UCSC Ensembl
chr7:135460327..135461136hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272609
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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