A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963970



Internal ID22738905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155142232..155142232hg38UCSC Ensembl
chr6:155463366..155463366hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412840
Samples
Known GenesTIAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963970
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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