A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557701



Internal ID20930772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107294030..107294760hg38UCSC Ensembl
chr7:106934475..106935205hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273586
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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