A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743952



Internal ID18718198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101102103..101108176hg38UCSC Ensembl
Outerchr9:101102084..101108201hg38UCSC Ensembl
Innerchr9:103864385..103870458hg19UCSC Ensembl
Outerchr9:103864366..103870483hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg386118
hg196118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545205
Supporting Variants
Samples
Known GenesLPPR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743952
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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