A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845916



Internal ID22620851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62276411..62286900hg38UCSC Ensembl
chr6:62986316..62996805hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3810490
hg1910490
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502344
Samples
Known GenesKHDRBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845916
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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