A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560674



Internal ID20933745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120635978..120825725hg38UCSC Ensembl
chr7:120276032..120465779hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38189748
hg19189748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272308
Samples
Known GenesKCND2, TSPAN12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560674
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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