A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885568



Internal ID22660552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100409559..100409615hg38UCSC Ensembl
chr2:101026021..101026077hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391365
Samples
Known GenesCHST10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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