A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467130



Internal ID22525021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27639017..27649271hg38UCSC Ensembl
chr14:28108223..28118477hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3810255
hg1910255
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852274
Supporting Variants
Samples
Known GenesLINC00645
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467130
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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