A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843738



Internal ID22618673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12563636..12647126hg38UCSC Ensembl
chr6:12563868..12647358hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3883491
hg1983491
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843738
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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