A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568560



Internal ID20941631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25120106..25121135hg38UCSC Ensembl
chr7:25159725..25160754hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381030
hg191030
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6623n223
Supporting Variantsnssv18273338
Samples
Known GenesCYCS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568560
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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