A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897176



Internal ID22672275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217216245..217222859hg38UCSC Ensembl
chr2:218080968..218087582hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg386615
hg196615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897176
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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