A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950492



Internal ID22725892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6906483..6906483hg38UCSC Ensembl
chr6:6906716..6906716hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950492
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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