A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6901759



Internal ID10011988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4017103..4017583hg38UCSC Ensembl
Outerchr16:4067104..4067584hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750422
Supporting Variants
SamplesSSM012
Known GenesADCY9
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)essv6901759
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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