A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4159n100



Internal ID22790246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207479254..207495060hg38UCSC Ensembl
chr2:208343978..208359784hg19UCSC Ensembl
chr2:208052223..208068029hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3815807
hg1915807
hg1815807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005120, nsv1003975
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)dgv4159n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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