A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633265



Internal ID6673387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96206868..96208304hg38UCSC Ensembl
Innerchr13:96206868..96208304hg38UCSC Ensembl
Outerchr13:96206767..96208441hg38UCSC Ensembl
chr13:96859122..96860558hg19UCSC Ensembl
Innerchr13:96859122..96860558hg19UCSC Ensembl
Outerchr13:96859021..96860695hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381437
hg191437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869276, essv14869275, essv14869277
SamplesNA19404, NA19377, NA19374
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633265
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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