A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868897



Internal ID22643832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43095207..43096818hg38UCSC Ensembl
chr2:43322345..43323956hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381612
hg191612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868897
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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