A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455764



Internal ID22513641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38871211..38873410hg38UCSC Ensembl
chr14:39340415..39342614hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853264
Supporting Variants
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455764
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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