A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833103



Internal ID22608038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6833035..6845909hg38UCSC Ensembl
chr2:6973166..6986040hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3812875
hg1912875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487645
Samples
Known GenesCMPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833103
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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