A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658785



Internal ID9924890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26334743..26335297hg38UCSC Ensembl
chr1:26661234..26661788hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5662530, essv6596271, essv6432689
SamplesNA18632, HG00418, NA19074
Known GenesAIM1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658785
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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