A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4891n100



Internal ID22790978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130067085..130109235hg38UCSC Ensembl
chr3:129785928..129828078hg19UCSC Ensembl
chr3:131268618..131310768hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3842151
hg1942151
hg1842151
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999468, nsv1008059, nsv1007581, nsv1001791, nsv1000952, nsv997867, nsv1001943, nsv1001988
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)dgv4891n100
Frequency
Sample Size11257
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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