A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6915777



Internal ID10026775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130268373..130272504hg38UCSC Ensembl
Outerchr9:133030652..133034783hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384132
hg194132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739098
Supporting Variants
SamplesSSM016
Known Genes
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)essv6915777
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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