A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836006



Internal ID22610941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46952118..46975287hg38UCSC Ensembl
chr3:46993608..47016777hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3823170
hg1923170
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492496
Samples
Known GenesCCDC12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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