A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431486



Internal ID21393488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28985647..28991341hg38UCSC Ensembl
chr11:29007194..29012888hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg385695
hg195695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n172
Supporting Variantsnssv15754301, nssv15747904, nssv15753807, nssv15750074, nssv15750926, nssv15754484, nssv15750457, nssv15748970, nssv15752201, nssv15748378
SamplesSMI034, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB07, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431486
Frequency
Sample Size15
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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