A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632304



Internal ID7019113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60635277..60651620hg38UCSC Ensembl
chr13:61209411..61225754hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3816344
hg1916344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14757001, essv14757002, essv14757006, essv14757003, essv14757005, essv14757000, essv14757004
SamplesHG03280, HG03126, NA19198, HG03343, HG02334, HG02817, NA19328
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632304
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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