A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558884



Internal ID20931955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99513440..99513902hg38UCSC Ensembl
chr7:99111063..99111525hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275855
Samples
Known GenesZKSCAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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