A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677316



Internal ID9943421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64812846..64914925hg38UCSC Ensembl
chr7:64273224..64375303hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38102080
hg19102080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6459174, essv5935627, essv6310349, essv6438309, essv6490794, essv5461333
SamplesNA12750, NA18595, NA18916, NA07347, HG00160, NA18548
Known GenesZNF138, ZNF273
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677316
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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