A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624428



Internal ID7011283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104344569..104348113hg38UCSC Ensembl
Innerchr10:104344569..104348113hg38UCSC Ensembl
Outerchr10:104344300..104348418hg38UCSC Ensembl
chr10:106104327..106107871hg19UCSC Ensembl
Innerchr10:106104327..106107871hg19UCSC Ensembl
Outerchr10:106104058..106108176hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg383545
hg193545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13917399, essv13917394, essv13917383, essv13917400, essv13917382, essv13917396, essv13917384, essv13917380, essv13917395, essv13917385, essv13917393, essv13917379, essv13917389, essv13917397, essv13917388, essv13917387, essv13917381, essv13917401, essv13917390, essv13917392, essv13917391, essv13917402, essv13917386, essv13917398
SamplesHG02890, HG03378, HG03175, HG03057, NA19734, HG03130, HG03190, HG03297, HG03193, HG03478, HG03074, NA19201, NA19138, NA19038, NA18977, NA19317, NA19462, NA18933, NA19984, HG03081, HG02455, NA19835, HG03433, NA19474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624428
Frequency
Sample Size2504
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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