A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556208



Internal ID20929279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98795429..98796766hg38UCSC Ensembl
chr7:98393052..98394389hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556208
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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