A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4898n100



Internal ID22790985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130072354..130137891hg38UCSC Ensembl
chr3:129791197..129856734hg19UCSC Ensembl
chr3:131273887..131339424hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3865538
hg1965538
hg1865538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011686, nsv1013342
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4898n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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