A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6762867



Internal ID9822515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:142751744..142762701hg38UCSC Ensembl
Outerchr7:142459595..142470550hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810958
hg1910956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2735272, esv2735271
Supporting Variants
SamplesSSM062
Known GenesPRSS1
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)essv6762867
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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