A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3849n100



Internal ID22789936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55095747..55118126hg38UCSC Ensembl
chr2:55322883..55345262hg19UCSC Ensembl
chr2:55176387..55198766hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3822380
hg1922380
hg1822380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997458, nsv1013316, nsv1004503, nsv1006172, nsv999212
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)dgv3849n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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