A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743356



Internal ID18370916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17144811..17145140hg38UCSC Ensembl
Outerchr9:17144793..17145158hg38UCSC Ensembl
Innerchr9:17144809..17145138hg19UCSC Ensembl
Outerchr9:17144791..17145156hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3544609
Supporting Variants
Samples
Known GenesCNTLN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743356
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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