A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6962395



Internal ID9721554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:10012696..11913136hg38UCSC Ensembl
Outerchr3:10054380..11954610hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381900441
hg191900231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2724892
Supporting Variants
SamplesSSM027
Known GenesATG7, ATP2B2, BRK1, CIDECP, FANCD2, FANCD2OS, GHRL, GHRLOS, HRH1, IRAK2, LINC00606, LINC00852, MIR885, SEC13, SLC6A1, SLC6A11, SLC6A1-AS1, TAMM41, TATDN2, VGLL4, VHL
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)essv6962395
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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