A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844908



Internal ID22619843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43630992..43633020hg38UCSC Ensembl
chr6:43598729..43600757hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382029
hg192029
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505809
Samples
Known GenesMAD2L1BP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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