A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6213n100



Internal ID20157829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10239..231133hg38UCSC Ensembl
chr7:10239..231133hg19UCSC Ensembl
chr7:52899..326216hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38220895
hg19220895
hg18273318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025027, nsv1034633
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6213n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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