A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633363



Internal ID6673485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101469479..101481605hg38UCSC Ensembl
Innerchr13:101469496..101481588hg38UCSC Ensembl
Outerchr13:101469462..101481622hg38UCSC Ensembl
chr13:102121830..102133956hg19UCSC Ensembl
Innerchr13:102121847..102133939hg19UCSC Ensembl
Outerchr13:102121813..102133973hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3812127
hg1912127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14879610, essv14879609, essv14879608, essv14879611, essv14879607
SamplesHG03640, HG02252, NA20524, HG03238, HG02790
Known GenesITGBL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633363
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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