A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv671n172



Internal ID22815045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256001..383000hg38UCSC Ensembl
chr6:256001..383000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38127000
hg19127000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434896, nsv4434897
SamplesNB12, NB08, BTQ038, NB10, BTQ055, SMI041, NB11, NB07, SMI018, NB09
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv671n172
Frequency
Sample Size15
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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