A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6754292



Internal ID9816638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:7883168..7883867hg38UCSC Ensembl
Outerchr5:7883281..7883980hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729709
Supporting Variants
SamplesSSM058
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)essv6754292
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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