A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2745406



Internal ID9979690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:2107224..2107756hg38UCSC Ensembl
Outerchr12:2216390..2216922hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6685046, essv6691558, essv6800174, essv6709451, essv6851104, essv6677773, essv6673094, essv6965714, essv6959197, essv6894607, essv6819647, essv6908814, essv6768463, essv6834847, essv6857135, essv6867094, essv6862326
SamplesSSM036, SSM027, SSM064, SSM087, SSM088, SSM041, SSM026, SSM089, SSM032, SSM031, SSM014, SSM086, SSM072, SSM082, SSM078, SSM034, SSM098
Known GenesCACNA1C
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)esv2745406
Frequency
Sample Size96
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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