A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968857



Internal ID22743792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34751376..34751376hg38UCSC Ensembl
chr20:33339179..33339179hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393747
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968857
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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