A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585031



Internal ID6972555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2767758..2802942hg38UCSC Ensembl
chr1:2684305..2719507hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3835185
hg1935203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9841891, essv9841896, essv9841892, essv9841895, essv9841898, essv9841894, essv9841897, essv9841890, essv9841899, essv9841893
SamplesHG01063, HG03224, HG02315, HG03363, NA19042, HG02256, NA19834, HG02308, NA20348, HG03303
Known GenesTTC34
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585031
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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