A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv665n172



Internal ID22815039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178239492..178239929hg38UCSC Ensembl
chr5:177666493..177666930hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4434575, nsv4434576
SamplesBTQ055, BTQ016
Known GenesCOL23A1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv665n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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