A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3852n100



Internal ID22789939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:56524439..56669836hg38UCSC Ensembl
chr2:56751574..56896971hg19UCSC Ensembl
chr2:56605078..56750475hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38145398
hg19145398
hg18145398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009860, nsv1005547
Samples
Known GenesRNU6-35P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3852n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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