A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469652



Internal ID22527542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83991757..83997435hg38UCSC Ensembl
chr14:84458101..84463779hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg385679
hg195679
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864074
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469652
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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