A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562029



Internal ID20935100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111740139..111740711hg38UCSC Ensembl
chr7:111380195..111380767hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273672
Samples
Known GenesDOCK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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