A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622325



Internal ID7009184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10292243..10294407hg38UCSC Ensembl
Innerchr10:10292264..10294386hg38UCSC Ensembl
Outerchr10:10292222..10294428hg38UCSC Ensembl
chr10:10334206..10336370hg19UCSC Ensembl
Innerchr10:10334227..10336349hg19UCSC Ensembl
Outerchr10:10334185..10336391hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13695778
SamplesHG00407
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622325
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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