A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2721803



Internal ID10305439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:239094131..239094775hg38UCSC Ensembl
Outerchr2:240015827..240016471hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6789663, essv6683246, essv6910548, essv6973268, essv6752953, essv6804794, essv6938160, essv6833027, essv6922246, essv6951054, essv6781397, essv6700148, essv6711054, essv6869086, essv6669760, essv6730071, essv6920995, essv6704264, essv6813578
SamplesSSM008, SSM039, SSM074, SSM042, SSM090, SSM047, SSM018, SSM029, SSM003, SSM031, SSM068, SSM040, SSM082, SSM015, SSM077, SSM022, SSM070, SSM025, SSM034
Known GenesHDAC4
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)esv2721803
Frequency
Sample Size96
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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