A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459760



Internal ID22517646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41058227..41095010hg38UCSC Ensembl
chr14:41527432..41564215hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3836784
hg1936784
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861766
Supporting Variants
Samples
Known GenesLOC644919
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459760
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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