A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624528



Internal ID7011381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109794212..109825964hg38UCSC Ensembl
Innerchr10:109794212..109825964hg38UCSC Ensembl
Outerchr10:109793712..109826464hg38UCSC Ensembl
chr10:111553970..111585722hg19UCSC Ensembl
Innerchr10:111553970..111585722hg19UCSC Ensembl
Outerchr10:111553470..111586222hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3831753
hg1931753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933220
SamplesNA18591
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624528
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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