A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585726



Internal ID6973247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35956172..35962462hg38UCSC Ensembl
chr1:36421773..36428063hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386291
hg196291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9901864, essv9901860, essv9901866, essv9901854, essv9901858, essv9901852, essv9901853, essv9901849, essv9901855, essv9901867, essv9901861, essv9901868, essv9901848, essv9901851, essv9901859, essv9901869, essv9901857, essv9901863, essv9901862, essv9901870, essv9901850, essv9901856, essv9901865
SamplesHG03121, NA19332, HG03518, HG03297, NA18616, NA19457, NA20287, NA19038, NA19471, HG02545, NA19451, NA19391, NA18516, HG02283, NA19320, NA19395, NA19375, NA19309, HG01551, NA19376, HG03313, NA19346, NA19431
Known GenesAGO3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585726
Frequency
Sample Size2504
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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