A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623059



Internal ID7009916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44254758..44255575hg38UCSC Ensembl
Innerchr10:44254785..44255548hg38UCSC Ensembl
Outerchr10:44254731..44255602hg38UCSC Ensembl
chr10:44750206..44751023hg19UCSC Ensembl
Innerchr10:44750233..44750996hg19UCSC Ensembl
Outerchr10:44750179..44751050hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764979, essv13764985, essv13764984, essv13764983, essv13764980, essv13764981, essv13764986, essv13764978, essv13764982
SamplesHG03280, HG03172, NA19038, HG02439, NA19347, HG03124, HG03123, HG03469, NA19360
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623059
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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