A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861018



Internal ID22635953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95978086..95982571hg38UCSC Ensembl
chr14:96444423..96448908hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384486
hg194486
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv614n209
Supporting Variantsnssv17470201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861018
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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