A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904821



Internal ID22679999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113009916..113009975hg38UCSC Ensembl
chr2:113767493..113767552hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904821
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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