A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884605



Internal ID22659588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62443720..62444004hg38UCSC Ensembl
chr2:62670855..62671139hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884605
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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