A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633636



Internal ID7020444
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14909868, essv14909872, essv14909869, essv14909870, essv14909871
SamplesHG00610, HG00629, HG00596, HG00404, NA12272
Known GenesRASA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633636
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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