A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870965



Internal ID22645902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2598192..2621721hg38UCSC Ensembl
chr2:2601964..2625493hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3823530
hg1923530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870965
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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