A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433924



Internal ID21395926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15803696..15805229hg38UCSC Ensembl
chr3:15845203..15846736hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381534
hg191534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv507n172
Supporting Variantsnssv15751380
SamplesNB07
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433924
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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