A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431576



Internal ID21393578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68963532..68964531hg38UCSC Ensembl
chr11:68731001..68732000hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748436, nssv15748922, nssv15747787, nssv15749352, nssv15746957, nssv15747574
SamplesNB12, BTQ038, NB10, BTQ016, NB07, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431576
Frequency
Sample Size15
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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