A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6490794



Internal ID9282394
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 Flag1
Merged StatusS
Merged Variantsesv2677316
Supporting Variants
SamplesNA12750
Known GenesZNF138, ZNF273
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6490794
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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