A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465793



Internal ID22523682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58143942..58148164hg38UCSC Ensembl
chr14:58610660..58614882hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg384223
hg194223
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856413
Supporting Variants
Samples
Known GenesC14orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465793
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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