A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2739584



Internal ID9973925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:6160138..6160444hg38UCSC Ensembl
Outerchr1:6220198..6220504hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6925674, essv6699589, essv6780850, essv6954717, essv6910025, essv6913986, essv6789134, essv6718798, essv6885974, essv6761844, essv6695565, essv6874690, essv6832585, essv6892306, essv6961534, essv6773423, essv6877660, essv6863939, essv6797434, essv6972311, essv6813158, essv6776924, essv6801607, essv6859169, essv6950535, essv6967913, essv6714227, essv6937659, essv6750583
SamplesSSM022, SSM007, SSM027, SSM092, SSM082, SSM006, SSM043, SSM088, SSM089, SSM025, SSM072, SSM016, SSM057, SSM039, SSM067, SSM077, SSM062, SSM093, SSM066, SSM028, SSM029, SSM073, SSM019, SSM096, SSM068, SSM015, SSM026, SSM098, SSM070
Known GenesCHD5
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)esv2739584
Frequency
Sample Size96
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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