A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750413



Internal ID10331383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3656006..3657151hg38UCSC Ensembl
Outerchr16:3706007..3707152hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6877037, essv6776389, essv6839091, essv6665449, essv6869920, essv6975151, essv6857959
SamplesSSM008, SSM083, SSM011, SSM087, SSM092, SSM029, SSM004
Known GenesDNASE1
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)esv2750413
Frequency
Sample Size96
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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