A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433923



Internal ID21395925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15803668..15805229hg38UCSC Ensembl
chr3:15845175..15846736hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381562
hg191562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv507n172
Supporting Variantsnssv15753914, nssv15751428, nssv15749704, nssv15752620, nssv15750737
SamplesSMI034, SMI041, NB11, MDQ025, NB09
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433923
Frequency
Sample Size15
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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