A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585515



Internal ID6973038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24851690..24858230hg38UCSC Ensembl
Innerchr1:24851711..24858209hg38UCSC Ensembl
Outerchr1:24851669..24858251hg38UCSC Ensembl
chr1:25178181..25184721hg19UCSC Ensembl
Innerchr1:25178202..25184700hg19UCSC Ensembl
Outerchr1:25178160..25184742hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386541
hg196541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9892063, essv9892064, essv9892081, essv9892078, essv9892079, essv9892061, essv9892057, essv9892070, essv9892077, essv9892053, essv9892060, essv9892075, essv9892052, essv9892054, essv9892051, essv9892080, essv9892055, essv9892062, essv9892074, essv9892065, essv9892082, essv9892083, essv9892076, essv9892069, essv9892072, essv9892059, essv9892068, essv9892067, essv9892071, essv9892056, essv9892066, essv9892058, essv9892073
SamplesNA19648, NA20891, HG04229, HG04060, HG02804, HG03792, HG04100, HG01945, NA07347, HG04070, HG01170, HG01525, HG01771, HG01709, NA21114, HG02737, HG01122, HG01790, HG03805, HG02604, HG03953, HG03745, HG00099, HG04239, NA12873, HG03869, HG00256, HG04080, NA20897, HG01302, HG01269, HG04061, HG03864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585515
Frequency
Sample Size2504
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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