A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453633



Internal ID22511507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41002801..41016443hg38UCSC Ensembl
chr14:41472006..41485648hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3813643
hg1913643
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858820
Supporting Variants
Samples
Known GenesLOC644919
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453633
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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