A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1174e214



Internal ID20122597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31139843..31176217hg38UCSC Ensembl
chr6:31107620..31143994hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3836375
hg1936375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3608528, esv3608530
SamplesHG02943, HG01880, HG01915
Known GenesCCHCR1, POU5F1, PSORS1C1, PSORS1C3, TCF19
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1174e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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