A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5591481



Internal ID9905385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101415876..101416985hg38UCSC Ensembl
chr7:101059157..101060266hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667662
Supporting Variants
SamplesNA20800
Known GenesCOL26A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5591481
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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