A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382988



Internal ID22440858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38298988..38299072hg38UCSC Ensembl
chr14:38768192..38768276hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382988
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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