A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431446



Internal ID21393448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12979024..12983317hg38UCSC Ensembl
chr11:13000571..13004864hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384294
hg194294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15745944
SamplesBTQ016
Known GenesLINC00958
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431446
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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