A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882929



Internal ID22657906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205128568..205128881hg38UCSC Ensembl
chr1:205097696..205098009hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882929
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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