A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429179



Internal ID22487049
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 StatusS
Merged Variantsnsv5964306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429179
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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