A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6834446



Internal ID9887610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:21191121..21209663hg38UCSC Ensembl
Outerchr9:21191120..21209662hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3818543
hg1918543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738276, esv2738274
Supporting Variants
SamplesSSM082
Known GenesIFNA10, IFNA7
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)essv6834446
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer