A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14683341



Internal ID1523768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31578032..31652880hg38UCSC Ensembl
chr13:32152169..32227017hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3874849
hg1974849
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631699
Supporting Variants
SamplesHG01396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14683341
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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