A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672333



Internal ID9938438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34907868..35229570hg38UCSC Ensembl
chr3:34949360..35271062hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38321703
hg19321703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6163018, essv6417867, essv6358132, essv5926847, essv5813550, essv5697613, essv5668604, essv6028260, essv5498786, essv6111307, essv5863133, essv6216823, essv5435985, essv5536537, essv6585147, essv5836783, essv6309601, essv5523789, essv5877470, essv5673507, essv5990015, essv6445012, essv5636703, essv6300845, essv5756039, essv6265551, essv5970171, essv6269285
SamplesHG01441, HG01462, HG00608, HG01359, HG01079, NA18599, NA18606, HG01461, HG00654, HG00693, HG00272, NA18574, HG00464, HG00740, HG00651, NA20828, HG00463, NA19003, NA18535, NA18628, NA18950, HG00607, HG01137, HG00620, NA18631, NA11843, NA19429, NA19074
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672333
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer