A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14709895



Internal ID3836458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42629205..42654455hg38UCSC Ensembl
Innerchr13:42629705..42653955hg38UCSC Ensembl
Outerchr13:42628205..42655455hg38UCSC Ensembl
chr13:43203341..43228591hg19UCSC Ensembl
Innerchr13:43203841..43228091hg19UCSC Ensembl
Outerchr13:43202341..43229591hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3825251
hg1925251
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631895
Supporting Variants
SamplesHG03472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14709895
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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