A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6670688



Internal ID9740192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:7883460..7883519hg38UCSC Ensembl
Outerchr5:7883573..7883632hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729709, esv2729710
Supporting Variants
SamplesSSM031
Known GenesMTRR
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)essv6670688
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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