A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2728868



Internal ID10312504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183552690..183554147hg38UCSC Ensembl
Outerchr4:184473843..184475300hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6869436, essv6910967, essv6730541, essv6893158, essv6826029, essv6790156, essv6774306, essv6786037, essv6826030, essv6777827, essv6762410, essv6786036, essv6956394, essv6670559, essv6926503, essv6730543, essv6956393, essv6837093, essv6700663, essv6852453, essv6814012, essv6725932
SamplesSSM083, SSM011, SSM039, SSM090, SSM047, SSM069, SSM062, SSM026, SSM019, SSM031, SSM067, SSM066, SSM007, SSM015, SSM080, SSM077, SSM070, SSM098
Known Genes
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)esv2728868
Frequency
Sample Size96
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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