A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947552



Internal ID22723059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25677894..25678250hg38UCSC Ensembl
chr14:26147100..26147456hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947552
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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