A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4829n100



Internal ID22790916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99941910..100185939hg38UCSC Ensembl
chr3:99660754..99904783hg19UCSC Ensembl
chr3:101143444..101387473hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38244030
hg19244030
hg18244030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010579, nsv1010897, nsv1008483
Samples
Known GenesCMSS1, FILIP1L, MIR3921, MIR548G, TMEM30C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4829n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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