A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951414



Internal ID22726776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122204831..122204831hg38UCSC Ensembl
chr6:122525977..122525977hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951414
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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