A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880312



Internal ID22655282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154996962..154997094hg38UCSC Ensembl
chr1:154969438..154969570hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880312
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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