A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633276



Internal ID6673398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96607606..96613355hg38UCSC Ensembl
Innerchr13:96607623..96613338hg38UCSC Ensembl
Outerchr13:96607589..96613372hg38UCSC Ensembl
chr13:97259860..97265609hg19UCSC Ensembl
Innerchr13:97259877..97265592hg19UCSC Ensembl
Outerchr13:97259843..97265626hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg385750
hg195750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869334, essv14869333
SamplesNA19434, HG02282
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633276
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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