A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898368



Internal ID22673481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234805649..234807524hg38UCSC Ensembl
chr2:235714293..235716168hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg381876
hg191876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1254n209
Supporting Variantsnssv17396222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898368
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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