A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6889069



Internal ID9936957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91159237..91159492hg38UCSC Ensembl
Outerchr1:91624794..91625049hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714684, esv2714696
Supporting Variants
SamplesSSM097
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)essv6889069
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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