A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458842



Internal ID22516724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38863661..38870860hg38UCSC Ensembl
chr14:39332865..39340064hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851860
Supporting Variants
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458842
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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