A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623508



Internal ID7010364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63414737..63419228hg38UCSC Ensembl
Innerchr10:63414799..63419167hg38UCSC Ensembl
Outerchr10:63414676..63419290hg38UCSC Ensembl
chr10:65174497..65178988hg19UCSC Ensembl
Innerchr10:65174559..65178927hg19UCSC Ensembl
Outerchr10:65174436..65179050hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384492
hg194492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13835158
SamplesNA18579
Known GenesJMJD1C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623508
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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