A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv94n172



Internal ID22814468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106190927..106191954hg38UCSC Ensembl
chr10:107950685..107951712hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4431151, nsv4431152, nsv4431150
SamplesNB12, SMI034, NB08, MDQ045, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB11, NB07, SMI018, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv94n172
Frequency
Sample Size15
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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