A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2844n100



Internal ID22788931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32016645..34009022hg38UCSC Ensembl
chr16:32027966..33811489hg19UCSC Ensembl
chr16:31935467..33718990hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381992378
hg191783524
hg181783524
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063163, nsv1067339, nsv1055280, nsv1056532, nsv1067331, nsv1065657, nsv1061104, nsv1056836, nsv1065049, nsv1066639, nsv1064411, nsv1064260, nsv1062289, nsv1064127, nsv1056671, nsv1055636, nsv1063059, nsv1065205, nsv1064191, nsv1064762, nsv1064198, nsv1066185, nsv1062501, nsv1066896, nsv1057904, nsv1067367, nsv1056745, nsv1063633, nsv1063455, nsv1066889, nsv1061743
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2844n100
Frequency
Sample Size11257
Observed Gain192
Observed Loss54
Observed Complex0
Frequencyn/a


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