A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661710



Internal ID9927815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150322298..150326705hg38UCSC Ensembl
chr6:150643434..150647841hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5821366, essv6020770, essv5834397, essv5436769, essv5864845, essv6022552, essv6058718, essv6358197, essv5776609, essv5778710, essv5747922, essv6444788, essv5799056, essv6557759, essv5610472, essv6119788, essv6411436, essv5560696, essv6372383, essv6324934, essv6104678, essv6274099, essv5426925, essv5462472, essv6495763, essv6475207, essv5493730
SamplesNA18502, NA19399, NA19374, NA19319, NA18489, NA18916, NA19197, NA19782, NA20336, NA19904, NA19384, NA19159, NA19239, HG01124, HG01149, NA19449, NA18499, NA18853, NA19099, NA18858, NA19712, NA19240, NA19835, NA19468, NA19102, NA18522, NA19153
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661710
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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