A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13700158



Internal ID3701974
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622399
Supporting Variants
SamplesNA20882
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13700158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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