A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631865



Internal ID7018674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41071201..41073207hg38UCSC Ensembl
Innerchr13:41071226..41073182hg38UCSC Ensembl
Outerchr13:41071176..41073232hg38UCSC Ensembl
chr13:41645337..41647343hg19UCSC Ensembl
Innerchr13:41645362..41647318hg19UCSC Ensembl
Outerchr13:41645312..41647368hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382007
hg192007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14704702
SamplesHG03708
Known GenesWBP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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