A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6950668



Internal ID10059892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156836544..156837025hg38UCSC Ensembl
Outerchr1:156806336..156806817hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718451
Supporting Variants
SamplesSSM025
Known GenesNTRK1
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)essv6950668
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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