A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622397



Internal ID6662567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13061275..13065130hg38UCSC Ensembl
Innerchr10:13061292..13065114hg38UCSC Ensembl
Outerchr10:13061259..13065147hg38UCSC Ensembl
chr10:13103275..13107130hg19UCSC Ensembl
Innerchr10:13103292..13107114hg19UCSC Ensembl
Outerchr10:13103259..13107147hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383856
hg193856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13697889, essv13697890, essv13697891
SamplesHG02360, NA18633, HG02396
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622397
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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