A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916606



Internal ID22691825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27819350..27824591hg38UCSC Ensembl
chr12:27972283..27977524hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg385242
hg195242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916606
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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