A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544610



Internal ID18399000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17178004..17178157hg38UCSC Ensembl
Outerchr9:17177997..17178160hg38UCSC Ensembl
Innerchr9:17178002..17178155hg19UCSC Ensembl
Outerchr9:17177995..17178158hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743357
Samples
Known GenesCNTLN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544610
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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