A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903237



Internal ID22678402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101009694..101037392hg38UCSC Ensembl
chr6:101457570..101485268hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3827699
hg1927699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903237
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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