A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845693



Internal ID22620628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63784709..63787458hg38UCSC Ensembl
chr6:64494602..64497351hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507263
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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