A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2732395



Internal ID9966714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7751673..7752301hg38UCSC Ensembl
Outerchr10:7793636..7794264hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6900370, essv6890960, essv6850622, essv6856646, essv6908501, essv6866693, essv6688009, essv6976489, essv6887736, essv6819262, essv6815157, essv6861946, essv6838302, essv6672584, essv6965201, essv6958666, essv6734949, essv6862831, essv6879244
SamplesSSM100, SSM083, SSM027, SSM011, SSM087, SSM097, SSM093, SSM088, SSM029, SSM096, SSM026, SSM089, SSM035, SSM031, SSM014, SSM086, SSM078, SSM077, SSM049
Known GenesKIN
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)esv2732395
Frequency
Sample Size96
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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