A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6949767



Internal ID9707831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9226274..9226684hg38UCSC Ensembl
Outerchr17:9129591..9130001hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715626
Supporting Variants
SamplesSSM024
Known GenesNTN1
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)essv6949767
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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