A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2721n100



Internal ID22788808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7862523..7930290hg38UCSC Ensembl
chr16:7912525..7980292hg19UCSC Ensembl
chr16:7852526..7920293hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3867768
hg1967768
hg1867768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036899, nsv1045484
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)dgv2721n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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