A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14881036



Internal ID4380684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103382006..103403032hg38UCSC Ensembl
Innerchr13:103382506..103402532hg38UCSC Ensembl
Outerchr13:103381006..103404032hg38UCSC Ensembl
chr13:104034356..104055382hg19UCSC Ensembl
Innerchr13:104034856..104054882hg19UCSC Ensembl
Outerchr13:104033356..104056382hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3821027
hg1921027
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633395
Supporting Variants
SamplesHG03907
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14881036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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