A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623154



Internal ID6663322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48368174..48372802hg38UCSC Ensembl
Innerchr10:48368174..48372802hg38UCSC Ensembl
Outerchr10:48368033..48372937hg38UCSC Ensembl
chr10:49576217..49580845hg19UCSC Ensembl
Innerchr10:49576217..49580845hg19UCSC Ensembl
Outerchr10:49576076..49580980hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384629
hg194629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796090
SamplesNA18633
Known GenesMAPK8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623154
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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