A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3933n100



Internal ID22790020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88833599..89314751hg38UCSC Ensembl
chr2:89133112..89614508hg19UCSC Ensembl
chr2:88914227..89395623hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38481153
hg19481397
hg18481397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999924, nsv1008011, nsv1012570, nsv1010359, nsv1011179
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3933n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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