A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964306



Internal ID22739241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109886572..109886572hg38UCSC Ensembl
chr6:110207775..110207775hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964306
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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