A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956566



Internal ID22731743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102419600..102419600hg38UCSC Ensembl
chr6:102867475..102867475hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956566
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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