A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6171n100



Internal ID20157787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161900345..162284816hg38UCSC Ensembl
chr6:162321377..162705848hg19UCSC Ensembl
chr6:162241367..162625838hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38384472
hg19384472
hg18384472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032914, nsv1033222
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6171n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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