A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6961887



Internal ID9721097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:247433490..247434183hg38UCSC Ensembl
Outerchr1:247596792..247597485hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2727751
Supporting Variants
SamplesSSM027
Known GenesNLRP3
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)essv6961887
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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