A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898561



Internal ID22673678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:134073005..134084386hg38UCSC Ensembl
chr2:134830576..134841957hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3811382
hg1911382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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