A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929885



Internal ID22705144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120122135..120122312hg38UCSC Ensembl
chr12:120559939..120560116hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929885
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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