A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633391



Internal ID7020200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103059429..103069934hg38UCSC Ensembl
Innerchr13:103059429..103069934hg38UCSC Ensembl
Outerchr13:103058929..103070434hg38UCSC Ensembl
chr13:103711779..103722284hg19UCSC Ensembl
Innerchr13:103711779..103722284hg19UCSC Ensembl
Outerchr13:103711279..103722784hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3810506
hg1910506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv364e214
Supporting Variantsessv14881028
SamplesHG02012
Known GenesSLC10A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633391
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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