A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3698n100



Internal ID22789785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:265970..313392hg38UCSC Ensembl
chr2:265970..313392hg19UCSC Ensembl
chr2:255970..303392hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3847423
hg1947423
hg1847423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998821, nsv1011955
Samples
Known GenesACP1, FAM150B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3698n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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