A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5880356



Internal ID8857759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2691073..2691662hg38UCSC Ensembl
chr7:2730707..2731296hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670827
Supporting Variants
SamplesNA19719
Known GenesAMZ1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5880356
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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