A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574479



Internal ID20947550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25224251..25236893hg38UCSC Ensembl
chr7:25263870..25276512hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3812643
hg1912643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273342
Samples
Known GenesNPVF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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