A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv40n68



Internal ID6317565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37692880..37882864hg19UCSC Ensembl
chr17:34946406..35136390hg18UCSC Ensembl
chr17:34946406..35136390hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv833442, nsv833443
Samples
Known GenesERBB2, MIR4728, NEUROD2, PGAP3, PNMT, PPP1R1B, STARD3, TCAP
Method
Analysis
Platform
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)dgv40n68
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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