A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633277



Internal ID6673399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96652292..96679649hg38UCSC Ensembl
Innerchr13:96652300..96679641hg38UCSC Ensembl
Outerchr13:96652284..96679657hg38UCSC Ensembl
chr13:97304546..97331903hg19UCSC Ensembl
Innerchr13:97304554..97331895hg19UCSC Ensembl
Outerchr13:97304538..97331911hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3827358
hg1927358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869336, essv14869335
SamplesHG03086, HG03378
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633277
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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