A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv952n100



Internal ID20152568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90321336..90845607hg38UCSC Ensembl
chr10:92081093..92605364hg19UCSC Ensembl
chr10:92071073..92595344hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38524272
hg19524272
hg18524272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036256, nsv1049931, nsv1052753
Samples
Known GenesHTR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv952n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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