A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844764



Internal ID22619699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155844841..155855166hg38UCSC Ensembl
chr6:156165975..156176300hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810326
hg1910326
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844764
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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