A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566816



Internal ID20939887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12550873..13575818hg38UCSC Ensembl
chr7:12590499..13615443hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381024946
hg191024945
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6582n223
Supporting Variantsnssv18272973
Samples
Known GenesARL4A, SCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566816
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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