A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv658n67



Internal ID6316926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105444457..105500664hg19UCSC Ensembl
chr2:104810889..104867096hg18UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv829588, nsv829596, nsv829591, nsv829593, nsv829594, nsv829590, nsv829595
SamplesAK18, NA18969, NA18542, NA18949, NA18968, AK10, AK12
Known GenesLOC100506421, POU3F3
Method
Analysis
Platform
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)dgv658n67
Frequency
Sample Size31
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer