A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619835



Internal ID6660021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17256980..17269409hg38UCSC Ensembl
Innerchr9:17256980..17269409hg38UCSC Ensembl
Outerchr9:17256480..17269909hg38UCSC Ensembl
chr9:17256978..17269407hg19UCSC Ensembl
Innerchr9:17256978..17269407hg19UCSC Ensembl
Outerchr9:17256478..17269907hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3812430
hg1912430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13411953, essv13411947, essv13411928, essv13411930, essv13411943, essv13411934, essv13411958, essv13411940, essv13411949, essv13411945, essv13411942, essv13411955, essv13411939, essv13411931, essv13411937, essv13411954, essv13411929, essv13411935, essv13411950, essv13411924, essv13411938, essv13411926, essv13411956, essv13411936, essv13411957, essv13411925, essv13411946, essv13411959, essv13411960, essv13411944, essv13411932, essv13411952, essv13411951, essv13411941, essv13411933, essv13411948, essv13411927
SamplesNA20281, HG03064, NA18501, HG02896, NA19430, NA19317, HG03046, NA19338, HG02676, NA19378, HG02760, HG03548, HG01101, NA18873, HG02895, HG03162, NA19914, HG02703, NA18856, NA19397, HG02643, NA18539, NA19129, HG02768, HG02429, HG02502, HG02624, HG03303, HG03367, HG03556, HG03074, HG03077, HG03060, HG03517, NA18519, HG03689, HG02610
Known GenesCNTLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619835
Frequency
Sample Size2504
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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