A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1094n67



Internal ID6317362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27119294..27295010hg19UCSC Ensembl
chr7:27085819..27261535hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv824038, nsv824040, nsv824041, nsv824039
SamplesNA18542, NA18968, AK10, AK6
Known GenesEVX1, HOTAIRM1, HOTTIP, HOXA1, HOXA10, HOXA10-HOXA9, HOXA11, HOXA11-AS1, HOXA13, HOXA2, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, LOC100133311, MIR196B
Method
Analysis
Platform
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)dgv1094n67
Frequency
Sample Size31
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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