A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987353



Internal ID21896696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205696081..205697559hg38UCSC Ensembl
chr2:206560805..206562283hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535848
Samples
Known GenesNRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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