A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881299



Internal ID22656274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15219860..15219937hg38UCSC Ensembl
chr2:15359984..15360061hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409342
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881299
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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