A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624531



Internal ID6664695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110025201..110037883hg38UCSC Ensembl
Innerchr10:110025226..110037858hg38UCSC Ensembl
Outerchr10:110025176..110037908hg38UCSC Ensembl
chr10:111784959..111797641hg19UCSC Ensembl
Innerchr10:111784984..111797616hg19UCSC Ensembl
Outerchr10:111784934..111797666hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3812683
hg1912683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13933246, essv13933245
SamplesHG00182, HG00379
Known GenesADD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624531
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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