A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv663n172



Internal ID22815037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173545913..173547747hg38UCSC Ensembl
chr5:172972916..172974750hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381835
hg191835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434566, nsv4434565
SamplesNB08, NB11, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv663n172
Frequency
Sample Size15
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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