A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902311



Internal ID22677468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3640284..3648109hg38UCSC Ensembl
chr6:3640518..3648343hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387826
hg197826
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902311
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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