A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622399



Internal ID6662569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13076696..13083865hg38UCSC Ensembl
Innerchr10:13076846..13083715hg38UCSC Ensembl
Outerchr10:13076546..13084015hg38UCSC Ensembl
chr10:13118696..13125865hg19UCSC Ensembl
Innerchr10:13118846..13125715hg19UCSC Ensembl
Outerchr10:13118546..13126015hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387170
hg197170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700158
SamplesNA20882
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622399
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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