A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3703n100



Internal ID22789790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3838382..3876759hg38UCSC Ensembl
chr2:3885972..3924349hg19UCSC Ensembl
chr2:3863847..3902224hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3838378
hg1938378
hg1838378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003752, nsv1005377
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)dgv3703n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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