A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6906817



Internal ID9982891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:36740195..36740985hg38UCSC Ensembl
Outerchr1:37205796..37206586hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746974
Supporting Variants
SamplesSSM001
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)essv6906817
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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