A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946944



Internal ID22722444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35779512..35779641hg38UCSC Ensembl
chr15:36071713..36071842hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384230
Samples
Known GenesDPH6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946944
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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