A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3932n100



Internal ID22790019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88833599..89284138hg38UCSC Ensembl
chr2:89133112..89583895hg19UCSC Ensembl
chr2:88914227..89365010hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38450540
hg19450784
hg18450784
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006445, nsv1010884, nsv1003123, nsv997528, nsv999164, nsv1010573, nsv1004920, nsv999166
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)dgv3932n100
Frequency
Sample Size11257
Observed Gain15
Observed Loss13
Observed Complex0
Frequencyn/a


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