A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4026n100



Internal ID22790113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97360488..97665171hg38UCSC Ensembl
chr2:98013814..98281634hg19UCSC Ensembl
chr2:97379953..97648066hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38304684
hg19267821
hg18268114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009263, nsv1003384, nsv1010167, nsv999627, nsv1010905
Samples
Known GenesACTR1B, ANKRD36B, COX5B, LOC100506076, LOC100506123
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4026n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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