A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622690



Internal ID7009548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26468407..26476691hg38UCSC Ensembl
Innerchr10:26468407..26476691hg38UCSC Ensembl
Outerchr10:26468233..26476912hg38UCSC Ensembl
chr10:26757336..26765620hg19UCSC Ensembl
Innerchr10:26757336..26765620hg19UCSC Ensembl
Outerchr10:26757162..26765841hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388285
hg198285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13728572
SamplesHG00543
Known GenesAPBB1IP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622690
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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