A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5406400



Internal ID9723861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:117375409..117379112hg38UCSC Ensembl
Outerchr7:117375372..117379162hg38UCSC Ensembl
Innerchr7:117015463..117019166hg19UCSC Ensembl
Outerchr7:117015426..117019216hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg383791
hg193791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675467
Supporting Variants
SamplesNA19474
Known GenesASZ1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5406400
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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