A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666672



Internal ID9932777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141578425..141584392hg38UCSC Ensembl
chr7:141278225..141284192hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385968
hg195968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6509379, essv5530039
SamplesNA12283, HG00312
Known GenesAGK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666672
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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