A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624808



Internal ID7011658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124380356..124385935hg38UCSC Ensembl
Innerchr10:124380358..124385933hg38UCSC Ensembl
Outerchr10:124380354..124385937hg38UCSC Ensembl
chr10:126068925..126074504hg19UCSC Ensembl
Innerchr10:126068927..126074502hg19UCSC Ensembl
Outerchr10:126068923..126074506hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385580
hg195580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963185, essv13963188, essv13963176, essv13963177, essv13963180, essv13963181, essv13963187, essv13963184, essv13963178, essv13963179, essv13963175, essv13963191, essv13963189, essv13963182, essv13963192, essv13963183, essv13963190, essv13963186, essv13963174
SamplesHG03100, HG02485, NA19023, NA19385, NA19239, HG03343, HG03382, HG01241, HG02010, NA19324, HG02580, HG03557, HG03565, HG03112, HG01556, NA18488, NA19312, NA19214, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624808
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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