A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410786



Internal ID21068339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93268911..93269224hg38UCSC Ensembl
chr6:93978629..93978942hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146797
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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