A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846024



Internal ID22620959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93417969..93419618hg38UCSC Ensembl
chr6:94127687..94129336hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503168, nssv17508539
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846024
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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