A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375558



Internal ID22601227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22894713..22895017hg38UCSC Ensembl
chr14:23363922..23364226hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5941864
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375558
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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