A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2849n100



Internal ID22788936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32069540..32292156hg38UCSC Ensembl
chr16:32080861..32303477hg19UCSC Ensembl
chr16:31988362..32210978hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38222617
hg19222617
hg18222617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058590, nsv1058813
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2849n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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