A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5573371



Internal ID9750488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85212456..85213719hg38UCSC Ensembl
chr7:84841772..84843035hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671151
Supporting Variants
SamplesNA19701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5573371
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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