A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6160n100



Internal ID22792247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147341405..147390746hg38UCSC Ensembl
chr6:147662541..147711882hg19UCSC Ensembl
chr6:147704234..147753575hg18UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3849342
hg1949342
hg1849342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016430, nsv1022283
Samples
Known GenesSTXBP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6160n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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