A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6856547



Internal ID10254375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130277830..130277903hg38UCSC Ensembl
Outerchr9:133040109..133040182hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739101, esv2739100, esv2739099
Supporting Variants
SamplesSSM087
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)essv6856547
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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