A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917974



Internal ID22693195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14826002..14826521hg38UCSC Ensembl
chr10:14868001..14868520hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355515
Samples
Known GenesCDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917974
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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