A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903499



Internal ID22678667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220230002..220230468hg38UCSC Ensembl
chr2:221094723..221095189hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903499
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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