A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904873



Internal ID22680052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47002764..47004564hg38UCSC Ensembl
chr6:46970501..46972301hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435405
Samples
Known GenesGPR110
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904873
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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