A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633279



Internal ID6673401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96693501..96695645hg38UCSC Ensembl
Innerchr13:96693519..96695628hg38UCSC Ensembl
Outerchr13:96693484..96695663hg38UCSC Ensembl
chr13:97345755..97347899hg19UCSC Ensembl
Innerchr13:97345773..97347882hg19UCSC Ensembl
Outerchr13:97345738..97347917hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869339, essv14869338
SamplesHG01668, HG03237
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633279
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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