A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv38n100



Internal ID19010406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15839166..15924038hg38UCSC Ensembl
chr1:16165661..16250533hg19UCSC Ensembl
chr1:16038248..16123120hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3884873
hg1984873
hg1884873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004140, nsv1011695
Samples
Known GenesFLJ37453, SPEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv38n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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