A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv507n172



Internal ID22814881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15803487..15805229hg38UCSC Ensembl
chr3:15844994..15846736hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381743
hg191743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4433921, nsv4433924, nsv4433923, nsv4433922, nsv4433920
SamplesNB12, SMI034, NB08, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB11, NB07, SMI018, MDQ025, NB09
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv507n172
Frequency
Sample Size15
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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