A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13963173



Internal ID5209497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124327586..124342851hg38UCSC Ensembl
Innerchr10:124327605..124342833hg38UCSC Ensembl
Outerchr10:124327568..124342870hg38UCSC Ensembl
chr10:126016155..126031420hg19UCSC Ensembl
Innerchr10:126016174..126031402hg19UCSC Ensembl
Outerchr10:126016137..126031439hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3815266
hg1915266
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624807
Supporting Variants
SamplesNA18618
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13963173
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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