A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5167n100



Internal ID22791254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34759898..34830233hg38UCSC Ensembl
chr4:34761520..34831855hg19UCSC Ensembl
chr4:34437915..34508250hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3870336
hg1970336
hg1870336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004107, nsv1002469, nsv1006183, nsv1009830, nsv1007691, nsv1000521, nsv1008505, nsv997564, nsv1006387, nsv1012983, nsv1004167, nsv1003534, nsv1002103, nsv1012383
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5167n100
Frequency
Sample Size11257
Observed Gain95
Observed Loss0
Observed Complex0
Frequencyn/a


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