A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5083n100



Internal ID22791170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3580899..3707900hg38UCSC Ensembl
chr4:3582626..3709627hg19UCSC Ensembl
chr4:3552424..3679425hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38127002
hg19127002
hg18127002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007094, nsv1009842, nsv999564
Samples
Known GenesLINC00955, LOC100133461
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5083n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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