A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2947124



Internal ID10966790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41227748..41237748hg38UCSC Ensembl
Innerchr17:39384000..39394000hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7216691
SamplesHuRef
Known GenesKRTAP9-3
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2947124
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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