A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6906524



Internal ID10020666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:155800244..155800336hg38UCSC Ensembl
Outerchr2:156656756..156656848hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2721001, esv2721002
Supporting Variants
SamplesSSM014
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)essv6906524
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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