A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869667



Internal ID22644602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99901885..99908374hg38UCSC Ensembl
chr2:100518347..100524836hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386490
hg196490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409229
Samples
Known GenesAFF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869667
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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