A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3709n100



Internal ID22789796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4663889..4684131hg38UCSC Ensembl
chr2:4711479..4731721hg19UCSC Ensembl
chr2:4689354..4709596hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3820243
hg1920243
hg1820243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003943, nsv998638
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)dgv3709n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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