A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6847572



Internal ID10246297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:100445292..100445702hg38UCSC Ensembl
Outerchr2:101061754..101062164hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2720437
Supporting Variants
SamplesSSM086
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)essv6847572
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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