A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841111



Internal ID22616046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130527499..130534348hg38UCSC Ensembl
chr5:129863192..129870041hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg386850
hg196850
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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