A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4885n100



Internal ID22790972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130062021..130166820hg38UCSC Ensembl
chr3:129780864..129885663hg19UCSC Ensembl
chr3:131263554..131368353hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38104800
hg19104800
hg18104800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998948, nsv1003813, nsv998714, nsv1014512
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)dgv4885n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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