A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4101n100



Internal ID22790188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167544739..167596377hg38UCSC Ensembl
chr2:168401249..168452887hg19UCSC Ensembl
chr2:168109495..168161133hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3851639
hg1951639
hg1851639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004326, nsv1008206
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)dgv4101n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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