A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv556n172



Internal ID22814930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3568274..3634273hg38UCSC Ensembl
chr4:3570001..3636000hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3866000
hg1966000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434374, nsv4434375, nsv4434376
SamplesNB12, SMI034, NB08, MDQ045, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB11, NB07, SMI018, MDQ025, NB09
Known GenesLINC00955
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv556n172
Frequency
Sample Size15
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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