A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622395



Internal ID6662565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13014261..13019056hg38UCSC Ensembl
Innerchr10:13014332..13018985hg38UCSC Ensembl
Outerchr10:13014190..13019127hg38UCSC Ensembl
chr10:13056261..13061056hg19UCSC Ensembl
Innerchr10:13056332..13060985hg19UCSC Ensembl
Outerchr10:13056190..13061127hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384796
hg194796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13697867, essv13697874, essv13697872, essv13697870, essv13697881, essv13697884, essv13697879, essv13697869, essv13697883, essv13697885, essv13697887, essv13697877, essv13697866, essv13697875, essv13697873, essv13697878, essv13697871, essv13697882, essv13697865, essv13697886, essv13697876, essv13697868, essv13697880
SamplesHG01098, HG02215, HG03009, NA12813, HG00138, HG00158, NA12005, HG00120, HG02490, HG01519, NA20812, HG02736, HG00232, HG03624, HG04062, HG01789, HG00708, HG01094, NA06985, HG01589, HG02651, HG00116, NA07056
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622395
Frequency
Sample Size2504
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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