A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663049



Internal ID9929154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110827071..110827269hg38UCSC Ensembl
chr13:111479418..111479616hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6531607, essv5918213, essv5830869, essv5918836, essv6473463, essv6179036, essv6333961, essv6585736, essv5963975, essv5502979, essv5847840, essv5950994, essv6101704, essv6207836, essv6274353, essv5436269, essv5948281, essv5914486, essv5870009, essv5669410, essv5978232, essv5832753, essv6345967, essv5695778, essv5616947, essv5925090, essv6017251, essv6509877, essv5844164, essv5875807, essv5807889, essv5784690
SamplesNA18530, NA18582, HG01365, NA18611, HG00281, HG00309, NA18557, HG00253, HG00443, HG00282, HG00328, HG00475, HG00436, HG00584, HG01073, HG00651, HG00250, NA18532, HG00140, HG00246, HG00473, HG00237, NA19360, HG00256, HG00662, HG00339, HG00111, HG00513, HG00421, NA18989, NA18623, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663049
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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