A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844975



Internal ID22619910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46398694..46400631hg38UCSC Ensembl
chr6:46366431..46368368hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505847
Samples
Known GenesRCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844975
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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