A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2749184



Internal ID10330154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104097953..104098304hg38UCSC Ensembl
Outerchr14:104564290..104564641hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv277e201
Supporting Variantsessv6920534, essv6792185, essv6867558, essv6916402, essv6912922, essv6788096, essv6800560, essv6724789, essv6953570, essv6966327, essv6838919, essv6828036, essv6713271, essv6905208, essv6732449, essv6857726, essv6851727, essv6783881
SamplesSSM083, SSM027, SSM045, SSM087, SSM013, SSM042, SSM047, SSM069, SSM089, SSM017, SSM086, SSM068, SSM072, SSM015, SSM016, SSM080, SSM070, SSM025
Known GenesASPG
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)esv2749184
Frequency
Sample Size96
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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