A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3704n100



Internal ID22789791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4153079..4176417hg38UCSC Ensembl
chr2:4200669..4224007hg19UCSC Ensembl
chr2:4178544..4201882hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3823339
hg1923339
hg1823339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003168, nsv1013942, nsv1013159, nsv1010855, nsv1006267, nsv998778, nsv1001575, nsv1010501, nsv1000843, nsv1007395
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)dgv3704n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss67
Observed Complex0
Frequencyn/a


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