A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431534



Internal ID21393536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45724626..45743366hg38UCSC Ensembl
chr11:45746177..45764917hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3818741
hg1918741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754339
SamplesNB11
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431534
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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