A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949925



Internal ID22725364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100428628..100428628hg38UCSC Ensembl
chr6:100876504..100876504hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412495
Samples
Known GenesSIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949925
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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