A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571856



Internal ID20944927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154871314..154881732hg38UCSC Ensembl
chr7:154663024..154673442hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3810419
hg1910419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273763
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571856
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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