A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv570n100



Internal ID22786657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210543944..210569682hg38UCSC Ensembl
chr1:210717288..210743026hg19UCSC Ensembl
chr1:208783911..208809649hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3825739
hg1925739
hg1825739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003105, nsv1014480
Samples
Known GenesHHAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv570n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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