A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662136



Internal ID9581555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23930426..24035232hg38UCSC Ensembl
Outerchr1:23930055..24035602hg38UCSC Ensembl
Innerchr1:24256916..24361722hg19UCSC Ensembl
Outerchr1:24256545..24362092hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38105548
hg19105548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5503809, essv6022055, essv6050165, essv5517465, essv5767080, essv6527098
SamplesHG01521, HG01518, HG01522, HG01519, HG01515, HG01516
Known GenesPNRC2, SRSF10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662136
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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