A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846446



Internal ID22621381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2032476..2084806hg38UCSC Ensembl
chr7:2072111..2124441hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3852331
hg1952331
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504722
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846446
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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