A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14909871



Internal ID1006559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114103946..114128371hg38UCSC Ensembl
chr13:114869421..114893846hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3824426
hg1924426
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633636
Supporting Variants
SamplesHG00629
Known GenesRASA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14909871
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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