A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3934n100



Internal ID22790021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88834106..89027892hg38UCSC Ensembl
chr2:89133619..89327389hg19UCSC Ensembl
chr2:88914734..89108504hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38193787
hg19193771
hg18193771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013664, nsv1012148, nsv1008153, nsv1008233, nsv1001016, nsv1003191, nsv1002275, nsv1001285, nsv1002497, nsv998657, nsv1004913, nsv1003064, nsv998108, nsv998510, nsv1003789, nsv1014400, nsv1008488, nsv1012750, nsv1006967, nsv1011889, nsv1013655
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)dgv3934n100
Frequency
Sample Size11257
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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