A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948344



Internal ID22723828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163603764..163603764hg38UCSC Ensembl
chr6:164024796..164024796hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423342
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948344
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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