A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432906



Internal ID21394908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10393944..10400943hg38UCSC Ensembl
chr1:10454001..10461000hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754583, nssv15753759
SamplesBTQ038, BTQ016
Known GenesPGD
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432906
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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