A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2730786



Internal ID9965103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:132275048..132275576hg38UCSC Ensembl
Outerchr5:131610741..131611269hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6767388, essv6854981, essv6963444, essv6793454, essv6774461, essv6841079, essv6896641, essv6926684, essv6704853, essv6918581, essv6790349, essv6854130, essv6727198
SamplesSSM027, SSM011, SSM064, SSM087, SSM009, SSM084, SSM017, SSM003, SSM066, SSM040, SSM007, SSM070, SSM099
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)esv2730786
Frequency
Sample Size96
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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