A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631824



Internal ID7018633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38809885..38820635hg38UCSC Ensembl
Innerchr13:38809885..38820635hg38UCSC Ensembl
Outerchr13:38809720..38820689hg38UCSC Ensembl
chr13:39384022..39394772hg19UCSC Ensembl
Innerchr13:39384022..39394772hg19UCSC Ensembl
Outerchr13:39383857..39394826hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3810751
hg1910751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14699372, essv14699373
SamplesHG03703, HG03894
Known GenesFREM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631824
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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