A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841734



Internal ID22616669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128959240..128970015hg38UCSC Ensembl
chr5:128294933..128305708hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3810776
hg1910776
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494811
Samples
Known GenesSLC27A6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841734
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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