A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14909142



Internal ID1015059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113734588..113747254hg38UCSC Ensembl
chr13:114437561..114450227hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3812667
hg1912667
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633616
Supporting Variants
SamplesHG00634
Known GenesGRK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14909142
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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