A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4006n100



Internal ID22790093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91917300..92117746hg38UCSC Ensembl
chr2:92105326..92305772hg19UCSC Ensembl
chr2:91469053..91669499hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38200447
hg19200447
hg18200447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013689, nsv1014930, nsv1010698
Samples
Known GenesACTR3BP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4006n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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