A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544588



Internal ID18745664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15553926..15562703hg38UCSC Ensembl
Outerchr9:15553003..15563703hg38UCSC Ensembl
Innerchr9:15553924..15562701hg19UCSC Ensembl
Outerchr9:15553001..15563701hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3810701
hg1910701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743335
Samples
Known GenesCCDC171
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544588
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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