A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432927



Internal ID21394929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11336944..11337943hg38UCSC Ensembl
chr1:11397001..11398000hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753249
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432927
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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