A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881032



Internal ID22656004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3515507..3515556hg38UCSC Ensembl
chr2:3519278..3519327hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403838
Samples
Known GenesADI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881032
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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