A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2791n100



Internal ID22788878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19929929..19964959hg38UCSC Ensembl
chr16:19941251..19976281hg19UCSC Ensembl
chr16:19848752..19883782hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3835031
hg1935031
hg1835031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047948, nsv1046472, nsv1044119, nsv1040686, nsv1048321, nsv1048863, nsv1040765, nsv1044188, nsv1042909, nsv1049205, nsv1035883, nsv1035382, nsv1041264, nsv1041359, nsv1038864, nsv1038833, nsv1038406, nsv1044741, nsv1049471, nsv1036876, nsv1053420, nsv1039178, nsv1040159, nsv1052523, nsv1054607, nsv1036033
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)dgv2791n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss177
Observed Complex0
Frequencyn/a


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