A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573556



Internal ID20946627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25120077..25121181hg38UCSC Ensembl
chr7:25159696..25160800hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6623n223
Supporting Variantsnssv18273337
Samples
Known GenesCYCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573556
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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