A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944896



Internal ID22720368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26113958..26114076hg38UCSC Ensembl
chr15:26359105..26359223hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944896
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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