A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv67e180



Internal ID22757477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41227775..41238044hg38UCSC Ensembl
chr17:39384027..39394296hg19UCSC Ensembl
chr17:36637553..36647822hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3810270
hg1910270
hg1810270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv990862, esv991633
SamplesHuRef
Known GenesKRTAP9-3, KRTAP9-8
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv67e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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