A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906836



Internal ID22682040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202787816..202793096hg38UCSC Ensembl
chr2:203652539..203657819hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400396
Samples
Known GenesICA1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906836
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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