A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2736369



Internal ID10320005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:2054865..2055307hg38UCSC Ensembl
Outerchr8:2002983..2003425hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6694808, essv6861537, essv6808848, essv6733254, essv6931085, essv6830707, essv6841796, essv6720028, essv6881839, essv6827001, essv6860120, essv6856106, essv6964654, essv6834307, essv6866281, essv6870230, essv6805875, essv6671995, essv6939628, essv6908195, essv6727682, essv6850078, essv6698295
SamplesSSM027, SSM075, SSM046, SSM011, SSM087, SSM038, SSM074, SSM088, SSM084, SSM090, SSM089, SSM094, SSM031, SSM044, SSM014, SSM086, SSM081, SSM082, SSM020, SSM007, SSM080, SSM037, SSM022
Known GenesMYOM2
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)esv2736369
Frequency
Sample Size96
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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