A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3841n100



Internal ID22789928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52985159..53063500hg38UCSC Ensembl
chr2:53212297..53290638hg19UCSC Ensembl
chr2:53065801..53144142hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3878342
hg1978342
hg1878342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000235, nsv1011257, nsv1014197
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)dgv3841n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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