A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380107



Internal ID22437977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87349636..87351492hg38UCSC Ensembl
chr14:87815980..87817836hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381857
hg191857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380107
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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