A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868252



Internal ID22643187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4789701..4895485hg38UCSC Ensembl
chr2:4837291..4943075hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38105785
hg19105785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868252
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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