A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13716152



Internal ID5961454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23412217..23419420hg38UCSC Ensembl
Innerchr10:23412218..23419420hg38UCSC Ensembl
Outerchr10:23412217..23419421hg38UCSC Ensembl
chr10:23701146..23708349hg19UCSC Ensembl
Innerchr10:23701147..23708349hg19UCSC Ensembl
Outerchr10:23701146..23708350hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg387204
hg197204
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622611
Supporting Variants
SamplesNA19377
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13716152
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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