A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460022



Internal ID22517908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38805463..38813670hg38UCSC Ensembl
chr14:39274667..39282874hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg388208
hg198208
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863716
Supporting Variants
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460022
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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