A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849447



Internal ID22624382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82827635..82831857hg38UCSC Ensembl
chr14:83293979..83298201hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg384223
hg194223
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849447
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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