A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899329



Internal ID22674458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155683614..155701819hg38UCSC Ensembl
chr2:156540126..156558331hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3818206
hg1918206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899329
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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