A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4988n100



Internal ID22791075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176159637..176198600hg38UCSC Ensembl
chr3:175877425..175916388hg19UCSC Ensembl
chr3:177360119..177399082hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3838964
hg1938964
hg1838964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013027, nsv1005105, nsv999935, nsv1011164, nsv1010113
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4988n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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