A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623236



Internal ID6663404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51881429..51882426hg38UCSC Ensembl
Innerchr10:51881446..51882409hg38UCSC Ensembl
Outerchr10:51881412..51882443hg38UCSC Ensembl
chr10:53641189..53642186hg19UCSC Ensembl
Innerchr10:53641206..53642169hg19UCSC Ensembl
Outerchr10:53641172..53642203hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13804926, essv13804927, essv13804925
SamplesHG02272, HG02308, HG01923
Known GenesPRKG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623236
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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