A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624821



Internal ID7011671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124923228..124924041hg38UCSC Ensembl
Innerchr10:124923228..124924041hg38UCSC Ensembl
Outerchr10:124922989..124924329hg38UCSC Ensembl
chr10:126611797..126612610hg19UCSC Ensembl
Innerchr10:126611797..126612610hg19UCSC Ensembl
Outerchr10:126611558..126612898hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963380, essv13963387, essv13963363, essv13963389, essv13963371, essv13963372, essv13963365, essv13963373, essv13963367, essv13963398, essv13963397, essv13963388, essv13963392, essv13963390, essv13963399, essv13963374, essv13963379, essv13963394, essv13963369, essv13963361, essv13963381, essv13963395, essv13963376, essv13963364, essv13963375, essv13963391, essv13963362, essv13963370, essv13963384, essv13963366, essv13963386, essv13963400, essv13963382, essv13963383, essv13963377, essv13963360, essv13963393, essv13963368, essv13963378, essv13963359, essv13963396, essv13963358, essv13963385
SamplesNA18881, HG03300, NA18486, NA20294, HG03172, NA19098, NA19314, HG03095, HG03385, NA19723, HG03342, HG01063, NA19137, NA19172, HG03380, HG02943, HG03160, HG02582, NA19984, HG01989, HG03081, HG02014, HG02968, HG03027, HG02537, NA19776, NA19654, HG01102, HG03301, NA19114, HG02817, HG02445, NA19320, NA19395, HG02896, HG01988, HG01190, NA19256, HG03437, NA19712, HG03473, NA19323, HG02051
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624821
Frequency
Sample Size2504
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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