A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv117n100



Internal ID20151733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16883096..16935740hg38UCSC Ensembl
chr1:17209591..17262235hg19UCSC Ensembl
chr1:17082178..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3852645
hg1952645
hg1852645
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007304, nsv1010217, nsv1003197, nsv1011151, nsv1014213
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv117n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss18
Observed Complex0
Frequencyn/a


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