A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940957



Internal ID22716373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42496457..42496591hg38UCSC Ensembl
chr15:42788655..42788789hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371318
Samples
Known GenesSNAP23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940957
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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