A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2738772



Internal ID9973113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92558898..92575337hg38UCSC Ensembl
Outerchr9:95321180..95337619hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3816440
hg1916440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6976281, essv6845606
SamplesSSM085, SSM029
Known GenesCENPP
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2738772
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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