A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569672



Internal ID20942743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108530101..108531341hg38UCSC Ensembl
chr7:108170545..108171785hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7046n223
Supporting Variantsnssv18273617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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