A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433624



Internal ID21395626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161277490..161284489hg38UCSC Ensembl
chr2:162134001..162141000hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746563
SamplesSMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433624
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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