A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622436



Internal ID7009295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15092115..15094199hg38UCSC Ensembl
Innerchr10:15092136..15094178hg38UCSC Ensembl
Outerchr10:15092094..15094220hg38UCSC Ensembl
chr10:15134114..15136198hg19UCSC Ensembl
Innerchr10:15134135..15136177hg19UCSC Ensembl
Outerchr10:15134093..15136219hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382085
hg192085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704059
SamplesHG02724
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622436
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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